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| Teva Pharmaceuticals USA |
Irvine |
CA |
9/4/2010
|
| Director, Maintenance |
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| Teva Pharmaceuticals USA |
Irvine |
CA |
9/4/2010
|
| Sr. Regulatory Compliance Auditor |
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| Teva Pharmaceuticals USA |
Irvine |
CA |
9/4/2010
|
| Principal Scientist I - Preformulation/Formulation Group Leader |
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| Teva Pharmaceuticals USA |
Irvine |
CA |
9/4/2010
|
| Validation Engineer I |
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| Agilent Technologies, Inc. US |
Chandler |
AZ |
9/4/2010
|
| Sales - Genomics Product Specialist |
| - Minimum BS/MS in Chemistry or a Life Sciences discipline, or equivalent.
- Solid self management and organizational and prioritization skills
- 5+ years related direct sales experience with a demonstrated track record of successfully selling against a quota.
- High level of experience in microarrays and/or NGS.
- Technical knowledge and domain knowledge in the research and diagnostic sector of the pharmaceutical industry (profit and not for profit. Knowledge of the cytogenetics market.
- Industry/Application expertise. Working knowledge of competitive products (specifications, value propositions, price points).
- Comfortable interfacing with senior managers within your customers.
- Demonstrated commercial selling skills. Strong business development and sales closing skills.
- Effective interpersonal communication and telephone sales skills.
- Must be able to travel up to 35% of the time.
Geo Location: Arizona (preferred) or Texas |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Senior Software Engineer |
| * Bachelors or Masters degree in computer science and/or physical science.
* More than 5 years experience in industry-related software development
* Experience in the following software fields
- Application development experience using Oracle and SQL databases and Schema Design
- Windows development using .NET, C#, and C++
- Experience with Windows Services, WCF, Web Services
- Experience in server side development
- Desired experience in MVVM & CAL, MSI, MSBuild and WIX
- Also desired are experiences in Search Technologies, Data Object Design and Data Warehousing |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Marketing Director - Life Sciences |
| Requires:
- BS in biology, biochemistry, molecular biology; related discipline or equivalent. Master or PhD preferred.
- 8+ years experience in marketing life science products.
- Demonstrated use of marketing skills and market knowledge to define and commercialize products that result in business success
- Experience in working with worldwide customers and is a strong advocate for customer focus and customer driven development
- Demonstrate ability to develop marketing plans that align with strategic objectives
- Ability to work independently to plan, prioritize workload, schedule time, assess and solve problems
- High proficiency in pricing and forecasting
- Must exhibit strategic thinking, teamwork, creativity, planning and organization, and flexibility
- Strong analytical and decision making skills
- Experience in working with global markets/customers an advantage
- Excellent written and oral communications skills and comfortable presenting to high level audiences both internally and externally
- Must have flexibility in working hours and available for 25% business travel
Geographic Location: Santa Clara, California |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Clinical Program Marketing Manager |
| Qualifications:
Scientific Credentials: Scientific Degree in Analytical Chemistry, Clinical Chemistry or similar field. PhD preferred.
Relevant Work Experience: 5+ years experience in a clinical testing laboratory, clinical industry and/or previous sales/marketing position in an analytical instrumentation business
Clinical Domain Expertise: Fluent in all aspects of clinical chemistry lab operations. Working knowledge of sample prep, chromatography and quantitative LC/MS is required.
Communication Skills: Excellent written, verbal, and presentation skills essential.
Teamwork: Ability to function effectively in a matrix structure. Track record of success driving cooperation among global cross-functional teams. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Software Engineer |
| Job Requirements:
? Strong C# programming experience.
? Experience using Microsoft Visual Studio and source management tools, such as Microsoft Team Foundation Server.
? Experience using DevExpress, WPF, or similar GUI toolset.
? Broad knowledge and experience using design patterns.
? Strong work ethic with focus on quality, follow-through, and attention to detail.
? Good communication skills.
? Experience synthesizing a cohesive system consisting of hardware, electronics, firmware, and software.
Education & Experience:
? Degree in computer science, engineering, or related field.
? 5+ years of technical experience.
? Experience developing production quality software.
? Experience with C++ desired.
? Experience with TCP/IP desired.
? Experience with embedded programming desired. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Clinical LC/MS Applications Champion |
| BS or PhD Degree (preferred) or equivalent in Chemistry, BioChemistry, Biology, or related field.
Minimum of 5 years relevant experience with typically 9-15 years practical experience.
The successful person for this position will:
Be comfortable with LC/MS analysis of peptides, steroids, amino acids, vitamins : sample preparation, instrument operation, data analysis, and data interpretation and processing.
Have the ability to use new LC/MS technology especially TOF and triple quadrupole technology.
Have familiarity with software tools to assist in data processing for the production of proof statements and application notes.
Have a good understanding of clinical MS analysis
Be an effective communicator , have good written English skills and be an effective team player.
Ability to lead and design the workload of other application personnel.
Geo Location: Santa Clara, CA |
| Agilent Technologies, Inc. US |
San Francisco |
CA |
9/4/2010
|
| LCMS Applications Scientist - Clinical |
| - PhD in Chemistry or Biology or Biochemistry or equivalent
- 5+ years hands-on experience in the field of Mass Spectrometry in a clinical setting
- Experience with a broad range of LCMS instrumentation
- Experience in a clinical setting required
- Excellent verbal, written and presentation communications skills
- Strong project management experience skills
- Available for flexible work schedule and business up to 50% business travel.
Agilent will not sponsor work authorization |
| Agilent Technologies, Inc. US |
Chandler |
AZ |
9/4/2010
|
| Product Marketing Engineer |
| - Bachelor degree in relevant science or engineering discipline; Ph.D. strongly preferred (e.g. Material Science, Life Sciences, Chemistry, Physics, Biology or Biophysics)
- 5+ years recent experience applying scanning electron microscopy to scientific, industrial and/or manufacturing problems; understanding of electron-specimen interactions
- Exceptional written and verbal communication skills; Ability to address a diverse audience is critical to the successful candidate
- Versatile interpersonal skills to communicate across geographies, cultures, organizational functions.
- Domestic and international travel required
- Ability to speak a second language highly desirable
Geo Location: Chandler, AZ |
| Agilent Technologies, Inc. US |
Anaheim |
CA |
9/4/2010
|
| Field Service Engineer- Los Angeles Area |
| Requires BS or MS Degree or equivalent and 3 or more year's relevant experience with the use,repair,troubleshooting of hardware, software applications support and routine preventative maintenance, qualification and verification of Agilent's Liquid Chromatographs and LC Mass Spectrometers. LCMS experience required.
Geographic Location: Los Angeles Area
Agilent will not sponsor work authorization for this position |
| Agilent Technologies, Inc. US |
Columbia |
MD |
9/4/2010
|
| Wireless Network Engineer - Application Support |
| ?Bachelors or Masters Degree in Electrical/Electronic or Computer Engineering and 5+ years applicable experience in Mobile Communication Systems and Networks (including cell phone and other mobile communications infrastructure).
?Knowledge of wireless protocols, including: UMTS, GPRS, GSM and CDMA technologies
?Strong Linux/Unix system administration experience.
?Experience with Central Office networking
?Experience with Perl and Shell Scripting
?Experience with end user, installation and commissioning of new systems within customer environments is highly desired.
?Knowledge of Network Signaling is preferred
?Strong interpersonal/relationship skills, solid written and verbal communications.
?US citizenship is required, based on customer requirements
?Current high level US Government Security Clearance -or- ability to process for and obtain high level US Government Security Clearance.
Position is in Columbia, Maryland area. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| R&D Bioinformatics, Senior Software Engineer |
| External Qualifications:
This dynamic position requires a MS degree in Computer Science or equivalent plus a minimum of 5+ years relevant experience with bioinformatics tools and procedures as applied to high-throughput computational pipelines.
Chosen candidate must have the following:
? 5+ years experience in C++, .NET, and Java
? Object oriented programming experience a plus
? Experience with: BLAST, BLAT and/or MOST
? Experience with SQL and/or Oracle database
? Knowledge of public biological databases, tools, and repositories is required
? Hands-on experience producing software in collaborative, multidisciplinary environment to solve problems in biological or other life science is highly desirable
? Experience with Image Analysis is a plus
Geographic Location: Bay Area, California (Santa Clara) |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| R&D Bioinformatics, Software Engineer |
| External Qualifications:
This dynamic position requires a MS degree in Computer Science or equivalent plus a minimum of 5+ years relevant experience with bioinformatics tools and procedures as applied to high-throughput computational pipelines.
Chosen candidate must have the following:
? 2+ years of experience in providing bioinformatics solution in next gen sequencing space.
? 5+ years experience in C++, .NET, and Java
? Object oriented programming experience a plus
? Experience with: BLAST, BLAT and/or MOST
? Experience with SQL and/or Oracle database
? Knowledge of public biological databases, tools, and repositories is required
? Hands-on experience producing software in collaborative, multidisciplinary environment to solve problems in biological or other life science is highly desirable
? Experience with Image Analysis is a plus
Geographic Location: Bay Area, California (Santa Clara) |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| RF Field Applications Engineer |
| Position requires Bachelors or Master Degree or equivalent and a minimum of 2-4yrs+ in an Applications Engineering or Sales Support role.
? Must be US citizen.
? Must have knowledge of RF and microwave products such as network analyzers, signal generators and spectrum analyzers.
? Candidate must be knowledgeable of competition and able to identify lockout specification (identify Agilent's competitive advantage over competition)
? Must be able to analyze customer requirements and recommend appropriate solutions
? Must possess excellent communication skills |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Sr.Engineer/Ass. Staff Engineer |
| B.S. degree in physics, chemistry, or electrical engineering or equivalent, plus a minimum of 7 years of related experience, or an equivalent combination of M.S or Ph.D. degree and experience. Advanced degree and minimum of 6 years of relevant experience required for Staff Engineer.
*NMR experience, NMR systems experience and good operating knowledge of VNMRJ are strongly preferred.
*Good RF, analog, and digital electronic experience and operation of related test equipment required. And/or experience with High Powered RF preferred
*Mechanical engineering and machine shop experience a plus.
*Unix/Linux operating knowledge, basic CAD experience, and knowledge of MS Office required.
Strong analytical and troubleshooting skills are required.
*Good verbal and written communications skills. |
| Agilent Technologies, Inc. US |
Columbia |
MD |
9/4/2010
|
| Program Manager |
| ? Bachelors or Masters Degree in Electrical Engineering or Computer Science or equivalent experience.
? Ten or more years experiance in the industry with five or more years as a Program/Project Manager
? Background in Wireless or IP networking preferred.
? Experience executing DoD programs throughout a milestone-oriented program life cycle.
? Track record of delivering quality solutions on time and delighting customers
? Mastery of Microsoft Project, Excel, Word, and Outlook
? Experience in new product, or novel system, development processes (e.g., software or hardware) as well as experience with life cycle support processes.
? Proven ability to work in a team, gain alignment among customers, teams, peers, partners, and management
? Proven ability to adapt to changing requirements in response to pressing customer needs
? Proven ability to prioritize and balance resources across multiple projects
? Experience with leading, planning, organizing, tracking and reporting for project teams and tasks
? Meticulously attentive to detail
? Experience with mentoring, staffing, and people development.
? PM Certification a plus, but not required. (Experience counts for more.)
? US Citizen with, or capable of obtaining, a high level security clearance. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| R&D Production Manager |
| This is a managerial position for NMR Cold Probe Production and NPI. The manager is responsible for overseeing the assembly and test of all production cold probes, and coordinating closely with development on specials. The manager will also be responsible for working closely with Cold Probe Development on the smooth introduction of new products into production.
List Minimum education, training and experience needed to perform this job:
1. 15 years experience with NMR probes
2. 5 years minimum supervisory experience
3. familiarity with cryogenic and vacuum systems
4. 10 years manufacturing/production engineer experience |
| Agilent Technologies, Inc. US |
Santa Rosa |
CA |
9/4/2010
|
| R&D FPGA Engineer |
| Key required skills:
? Bachelors or Masters Degree or University Degree in Electrical Engineering and 5+ years applicable experience in FPGA design
? Ability to use FPGA simulation and design tools to realize and verify high quality and robust solutions in Verilog or VHDL.
? Experience with Xilinx ISE, including Plan Ahead, and synthesis tools, such as Synplify
? Ability to perform characterization and testing of design prototypes, and analyze and validate the design to meet product performance specifications.
? Strong interpersonal/relationship skills, solid written and verbal communication skills
Desired skills:
? Educational emphasis or work experience with signal processing theory, applications and development
? Skills in signal processing algorithm development and implementation using FPGAs
? Experience with team-based FPGA development ? design partitioning and integration
? Knowledge in high-speed digital design, PCI Express, DMA, memory systems |
| Agilent Technologies, Inc. US |
Everett |
WA |
9/4/2010
|
| R&D Signal Processing Software Engineer |
| Key Required Skills:
? Bachelors or Masters Degree or University Degree in Electrical Engineering or Computer Science
? Must have 5+ years applicable experience in software development involving signal processing theory, techniques and algorithm development
? Must have experience with the use of computer tools for simulation
? Must have demonstrated proficiency with C/C++ or C# programming languages
? Strong interpersonal/relationship skills, solid written and verbal communication skills
Additional Desired Skills:
? Proficiency with C#,.Net, Visual Studio, defect tracking, revision control, real-time systems and software/firmware lifecycles. |
| Agilent Technologies, Inc. US |
Everett |
WA |
9/4/2010
|
| R&D Hardware Control Software Engineer |
| This is a key SW development role.
Key Required Skills:
? Bachelors or Masters Degree in Electrical Engineering or Computer Science
? 3+ years applicable experience in software development involving hardware control and IO
? Must have proficiency with C#, C++, .Net, Visual Studio, defect tracking, revision control and software/firmware lifecycles
? Strong interpersonal/relationship skills, solid written and verbal communication skills
Additional Desired Skills:
? Familiarity with Windows device drivers
? Experience with the Windows Presentation Foundation graphical subsystem
? Educational emphasis or work experience with signal processing theory, applications and development |
| Agilent Technologies, Inc. US |
Santa Rosa |
CA |
9/4/2010
|
| Manufacturing Engineer |
| B.S. or M.S. in Chemistry, Chemical Engineering, Materials Science, Physics or equivalent experience.
Analytical Chemistry experience is essential and electroplating, chemical milling and/or materials science experience is highly desirable.
Experience with statistical process control and design of experiments is desired.
Candidates should have excellent interpersonal, problem solving, and communication skills.
US Citizenship/Permanent Resident status is highly recommended, but applications from highly qualified candidates requiring work sponsorship will also be considered.
Candidates requiring work sponsorship must be eligible for access to export controlled technology. |
| Agilent Technologies, Inc. US |
Newport |
DE |
9/4/2010
|
| Manufacturing Operations Coordinator |
| Musts:
- Demonstrated ability to work in a team environment.
- Demonstrated strong communication and organizational skills.
- Demonstrated ability to read and understand written procedures and instructions.
- Demonstrated ability to perform basic math (add, subtract, multiply, divide, ratios, weights & measures).
- Demonstrated ability to make timely decisions.
- Experience with troubleshooting and applying corrective actions.
- Demonstrated ability to maintain accurate records.
- Experience working with computers: keyboarding, Windows environment.
- Demonstrated ability to manipulate small parts, manual dexterity.
- Required to bend, stoop, and reach.
- Required to remain standing for extended periods of time.
- No known allergies to chemicals used in the work area.
- May be required to lift materials per entity specified and approved limits.
- May be required to participate in medical/screening or monitoring programs.
Desired:
- Basic PC skills: spreadsheets, word processing, databases.
- Previous manufacturing experience in an ISO certified environment. |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
9/4/2010
|
| Manufacturing Technician |
| You must have extensive experience with thick film screen printing or semiconductor photolithography/etch. 2 year-degree with minimum 7 years experience, 9?15 years preferred |
| Agilent Technologies, Inc. US |
Santa Rosa |
CA |
9/4/2010
|
| IC Product Engineer |
| M.S. or Ph.D. in Electrical Engineering, Materials Science or equivalent experience. Experience with advanced III-V semiconductor device fabrication, characterization and reliability is essential. Specific experience in high speed/frequency GaAs, InP and GaN device physics and RF microwave engineering is highly desirable. Experience with statistical process control and design of experiments is required. Candidates should have excellent interpersonal and communication skills for successful inter-group and intra-group interactions. This engineer must be highly motivated in order to accomplish all the tasks required to meet very aggressive product development schedules and world class manufacturing expectations.
Agilent will not sponsor work authorization for this position |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| GC/MS General Manager |
| COMPETENCIES REQUIRED
? General Management and proven Leadership Skills in a Complex, Global Environment. The GM will have demonstrated his/her ability to lead an organization by setting and meeting goals and motivating performance, despite obstacles and setbacks. Experience in coordinating, motivating and leading a multifunctional, dispersed team within a global large organization is essential. Expertise in creating compelling business plans and presentations for internal and external audiences is required. Similarly, it is essential this individual have good financial management skill and an ability to work closely with finance professionals in preparing strategic business plans.
? Relevant Industry/Scientific Understanding. This individual will have demonstrated current understanding and working knowledge of analytical instrumentation tools for the Chemical Analysis laboratories.
? Customer Relationship Orientation. S/he will have demonstrated insight into customers, their businesses, needs and values. Commitment to customers and building strong, long-term customer relationships will be of critical importance. An ability to leverage existing distribution channels, and to establish strategic partnership with the sales and marketing team will be key.
? Open and Effective Communicator with Strong People Skills. This candidate must have 5-10 years of people management experience, including experience in managing a team of managers. S/he will have the ability to build strong and open working relationships characterized by mutual respect and an ability to build valuable business relationships outside the organization. The individual will be skilled at communicating ideas to others and inviting and considering input from others. S/he will be accessible and approachable, respecting intellectual integrity and valuing individuality. This individual will be skilled in hiring, motivating and developing talent.
? Education. An advanced degree in the business, engineering or science with an MBA from a well-regarded institution would be ideal.
- Location: Santa Clara, CA |
| Agilent Technologies, Inc. US |
San Diego |
CA |
9/4/2010
|
| Manufacturing Tech |
| Qualifications (Includes education, certifications, experience, etc.):
· Must have 5 years electrical and electronic maintenance experience.
· Must demonstrate skills/experience in electrical wiring and troubleshooting.
· Must have Knowledge and experience with digital and conventional controls systems, including Allen Bradley PLC and Wonderware control system.
· Must have the ability to read and interpret drawings and schematics.
· The ability to interact/coordinate with service contractors, engineering professionals, and vendors is preferred.
· Valid California Drivers License
· Good computer skills, including knowledge of Word, Excel and e-mail programs.
Physical Demands:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this Job, the employee is regularly required to stand; walk; use hands to finger, handle, or feel and reach with hands and arms. The employee is occasionally required to sit and talk or hear. Employees must be able to lift up to 50lbs and be able to safely manipulate heavier objects using material handling equipment, such as pallet jacks, dollies and forklifts. Specific vision abilities required by this job include close vision, color vision, peripheral vision, depth perception and ability to adjust focus. Personal protective equipment used may include: safety goggles/glasses, lab coat, earplugs, hairnet, if welding, welding jacket and mask, dust mask and respirator.
Work Environment:
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is regularly exposed to moving mechanical parts. The location of the task may require the employee to use various size ladders and be exposed to different heights. The noise level in the work environment is usually moderate. Depending on the complexity of the problem, associate will work in an environment with exposure to grease, dirt, oil and some chemicals.
GEOGRAPHIC LOCATION: LAKE FOREST, CA
NO RELOCATION OR SPONSORSHIP FOR THIS ROLE |
| Agilent Technologies, Inc. US |
Newport |
DE |
9/4/2010
|
| Manufacturing Operations Coordinator |
| Musts:
- Demonstrated ability to work in a team environment.
- Demonstrated strong communication and organizational skills.
- Demonstrated ability to read and understand written procedures and instructions.
- Demonstrated ability to perform basic math (add, subtract, multiply, divide, ratios, weights & measures).
- Demonstrated ability to make timely decisions.
- Experience with troubleshooting and applying corrective actions.
- Demonstrated ability to maintain accurate records.
- Experience working with computers: keyboarding, Windows environment.
- Demonstrated ability to manipulate small parts, manual dexterity.
- Required to bend, stoop, and reach.
- Required to remain standing for extended periods of time.
- No known allergies to chemicals used in the work area.
- May be required to lift materials per entity specified and approved limits.
- May be required to participate in medical/screening or monitoring programs.
Desired:
- Basic PC skills: spreadsheets, word processing, databases.
- Previous manufacturing experience in an ISO certified environment. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Surveillance Application Engineer |
| Bachelors or Master Degree or University Degree or equivalent plus a minimum of 3 years relevant experience, with typically 5 to 8 years practical experience. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Reliability Engineer |
| You will need to have a university degree level or equivalent (complemented by a post-graduate degree and/or certification/license). You'll also bring at least 8 years' relevant experience. An accomplished leader and influencer, Agilent is where your expertise and solutions oriented approach will take you even further.
Required Qualifications:
1. BS in Engineering / Science or equivalent with a minimum of 8 years of relevant functional experience in Reliability and Quality.
2. Post Graduate and / or certification may be required.
3. Demonstrated strong communication skills particularly around the ability to translate reliability terms and concepts such as MTBF, AFR, and ALT into objectives that engineering teams can relate to and understand.
4. Demonstrated skill in teamwork within an organization and across sites as a proactive partner.
5. Demonstrated ability to provide leadership through credibility with R&D teams based on knowledge of reliability planning, relevant testing and customer advocacy.
6. Demonstrated results orientation/accountability. Ability to remain objective given conflicting or missing information and ability to identify what should be done to fill the Gap.
7. Demonstrated skill in planning and organization particularly as it applies to judgment of priorities while managing multiple projects and tasks.
This position is located in Santa Clara, CA |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| R&D engineer |
| Qualifications:
- Bachelor/Master/PhD Degree in Electrical/Electronic/Computer Engineering with >5 years related working experience
- Experience with Xilinx ISE, ModelSim, Synplify
- Experience with VHDL or Verilog
- Experience using equipment like oscilloscopes and logic analyzers for problem resolution and design verification
You will be measured on:
Technical capability and competence and ability to grow and remain technically current
Creativity in designing applicable solutions
Ability to work with a team to deliver results as committed |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| R&D Hardware Engineer |
| Qualifications:
- Bachelor/Master/PhD Degree in Electrical/Electronic/Computer Engineering with >3 years related working experience
- Knowledgeable in PCIe/modular busses, high-speed digital and memory systems, power integrity, thermal management
- Strong knowledge of digital design with emphasis on ASICs or Xilinx FPGAs
Desired:
- Nano technology/surface science or instrumentation measurement science/domain knowledge
- Strong knowledge of digital and analog hardware, FPGA or digital ASIC development principles, Verilog or VHDL, synthesis, and simulation tools.
- Knowledge of Xilinx ISE, Plan Ahead
- Knowledge of distributed clocking schemes
You will be measured on:
Technical capability and competence and ability to grow and remain technically current
Creativity in designing applicable solutions
Ability to work with a team to deliver results as committed |
| Agilent Technologies, Inc. US |
Albuquerque |
NM |
9/4/2010
|
| Field Service Engineer- Albuquerque |
| Requires BS or MS Degree or equivalent and 2 or more years relevant experience with the use, repair, routine preventative maintenance, qualification and verification of Agilent LSCA products including GC Mass Spectrometers, Gas Chromatographs, Liquid Chromatographs,GC Headspace, and Chemstation Data Systems.
Must have GC and GCMS experience.
Desired LC and ICPMS experience
Geographic Location: Albuquerque, New Mexico |
| Agilent Technologies, Inc. US |
Indianapolis |
IN |
9/4/2010
|
| Product Specialist - Columns and Supplies - Midwest |
| - BS Degree in Science (Chemistry/Biology) or equivalent
- 8+ years progressive experience in chromatography applications and/or sales along with a demonstrated track record of results preferred.
- Proven ability to understand customer needs and identify solutions to non-standard tasks/queries; actively creates business opportunities.
- Ability to solve a broad range of problems of varying scope and complexity.
- Excellent communication and teamwork skills is a must.
Geo Location: Midwest Area |
| Agilent Technologies, Inc. US |
Newport |
DE |
9/4/2010
|
| Chemical Process Operator |
| - Technical Associate degree or equivalent experience
- 3 to 5 years of laboratory or industrial chemical experience
- Demonstrated ability to work in a team environment
- Demonstrated strong written and oral communication and organization skills
- Experience setting up process or laboratory equipment
- Demonstrated ability to read and understand written procedures and instructions
- Demonstrated ability to maintain accurate and detailed records
- Demonstrated ability to perform basic math (add, subtract, multiply, divide, ratios, weights and measures)
- Demonstrated ability to work safely with potentially hazardous materials
- Demonstrated ability to efficiently perform job responsibilities with little daily supervision & to make timely decisions
- Demonstrated ability to adjust rapidly and effectively to change and to remain open to new ideas
- Demonstrated ability to troubleshoot issues and apply corrective actions
- Required to bend, stoop, reach, and to remain standing for extended periods of time
- Required to lift up to 50 lbs
- No known allergies to chemicals used in the work area
- May be required to participate in medical screening or monitoring programs |
| Agilent Technologies, Inc. US |
La Jolla |
CA |
9/4/2010
|
| Wireless Systems Application Engineer |
| Qualifications:
? BSEE or Masters degree in Engineering
? 5+ years hands-on experience with RF instrumentation including Spectrum Analyzers, Signal Sources, Power Meters
? 5+ years experience with Agilent Signal Studio, Agilent Vector Signal Analyzer, Matlab, or equivalent competitor design tools
? 3+ years hands-on R&D/development experience in Layer 1 (PHY) Wireless technologies such as GSM, GPRS, EGPRS, WCDMA (UMTS), HSPA, CDMA2000, 1xEVDO
? 3+ years hands-on experience with Cellular OBT?s such as Agilent 8960, R&S CMU200, Anritsu MT8820
Additional Skills:
? Familiarity with 3GPP, 3GPP2 (e.g. TS51.010, 34.121) test specifications
? Computer/IT admin skills; general system administration, setup, networking, and configuration mgt skills
? Software expertise; VB6, .NET, C#, Labview, scripting
? RF simulators; ADS, SystemVue
? Good customer communication skills; ability to lead customer facing technical discussions
? Office Tools; MS Word, Powerpoint, Excel, Visio, etc
? Excellent problem solving, diagnostic skills
? Strong trouble-shooting skills
? Strong team player |
| Agilent Technologies, Inc. US |
Newport |
DE |
9/4/2010
|
| Material Coordinator-2nd shift |
| May require some higher education or specialized training/certification.
Requires a minimum of 3 years directly related experience, with typically 4 to 6 years' experience.
Musts:
- Demonstrated ability to work in a team environment.
- Demonstrated strong communication and organizational skills.
- Demonstrated ability to read and understand written procedures and instructions.
- Demonstrated ability to perform basic math (add, subtract, multiply, divide, ratios, weights & measures).
- Demonstrated ability to make timely decisions.
- Demonstrated ability to maintain accurate records.
- Experience working with computers: keyboarding, Windows environment, spreadsheets, word processing, databases.
- Demonstrated ability to manipulate small parts, manual dexterity.
- Required to bend, stoop, and reach.
- Required to remain standing for extended periods of time.
- No known allergies to chemicals used in the work area.
- Required to lift materials per entity specified and approved limits.
- May be required to participate in medical/screening or monitoring programs.
Desired:
- Previous experience using SAP in a material coordination capacity.
- Previous manufacturing experience in an ISO certified environment |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Senior Product Manager / Life Sciences Marketing |
| ? 5+ years of product marketing/management experience; services marketing experience a plus
? Familiarity with Life Sciences industry and analytical instrumentation
? Track record of successful business results
? Bachelors degree in chemistry, biology or related scientific field or equivalent; MBA a plus
? Experience in leading cross-functional and international project teams
? Excellent verbal and communication skills
? Ability to travel, including international, approximately 35% of the time
? Physical work location at a major Agilent site (Santa Clara, CA or Wilmington, DE or Englewood, CO) strongly preferred |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Senior Product Manager |
| ? Minimum bachelors degree in chemistry, biology or related scientific field or equivalent; MBA a plus
? Minimum 4 years of product marketing experience; strong preference for Services Marketing experience
? Minimum of 3 years experience in marketing, selling, commercializing, managing, supporting analytical lab instrumentation or analytical lab experience, preferably in the Life Sciences industry
? Track record of business results
? Strong evidence of customer orientation
? Demonstrated ability to influence all levels of an organization, across regional/cultural boundaries and across multiple disciplines
? Excellent verbal & written communication skills.
? Ability to travel, including international
(10-30%)
Location: In Santa Clara, CA, Wilmington, DE, Englewood, CO |
| Agilent Technologies, Inc. US |
Tigard |
OR |
9/4/2010
|
| Account Manager |
| Bachelors or Master Degree in engineering (Electrical Engineering is a plus) and a minimum of 5+ years as a strategic Account Manager
Experience selling digital & wireless test products
Strong knowledge and Experience dealing with customers in the computer, wireless, and data networking industries
The candidate must live in close proximity to Portland, Oregon |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Mixed-Signal/RF IC Designer |
| Education:
Ph.D. in Electrical Engineering or closely related field with thesis work on mixed-signal IC design preferred. Candidates should have designed, have had fabricated and characterized a mixed-signal or RF integrated circuit as a central portion of their relevant thesis work.
M.S. in Electrical Engineering with experience in or substantial coursework related to mixed-signal IC design required. Candidates not possessing a Ph.D. degree must have completed the design, have had fabricated and characterized a mixed-signal or RF integrated circuit of complexity and performance commensurate with that of a Ph.D. thesis. In addition, two years relevant full-time employment experience or full-time graduate study is required post M.S. degree.
Qualifications:
Must have experience in the design of high-speed analog, mixed-signal or RF integrated circuits.
Substantial involvement in the design of transistor level circuits for inclusion on an IC, physical design of ICs, and the test and characterization of an IC.
Strong understanding of transistor physics and EM theory and their impact on circuits. Experience in 2-D and 3-D electromagnetic simulation of on-chip structures and derivation of a model for use in circuit simulators is highly desired.
Ability to synthesize multiple solutions to a given problem and the ability to critically analyze the strengths and weaknesses of each.
Experience with modern EDA tools used in IC design including simulation, schematic capture, physical layout and verification.
Familiarity with programming and scripting languages to enable automation in the design, simulation and testing of ICs.
Demonstrated ability to work well in a team environment is a must. Ability to document and present results.
Preferred Qualifications:
Experience with the use of both sub-micron CMOS and modern SiGe bipolar devices (fT > 150 GHz) in analog, mixed-signal, or RF integrated circuit design.
Experience with PLLs, clock-data recovery circuits, and data converters.
Experience with custom high-speed digital data paths.
Experience with a synthesized digital design flow, from a high-level HDL to transistor level artwork.
Experience with mixed-mode simulation of analog and digital blocks -- mixed-signal or behavioral modeling of analog circuits.
Experience with device modeling, thermal design, IC package design. |
| Agilent Technologies, Inc. US |
Cary |
NC |
9/4/2010
|
| Production Manufacturing Supervisor |
| ? Will have a bachelor?s degree in a technical or operational field.
? Will have a minimum of five years of experience as supervisor preferably in high precision technology product manufacturing.
? Extensive knowledge of lean manufacturing process activities and quality management system requirements.
? Proficiency with SAP or other ERP systems and Microsoft Office Applications.
? Proficiency in verbal and written English. |
| Agilent Technologies, Inc. US |
Englewood |
CO |
9/4/2010
|
| Application Engineer |
| Agilent is looking for new college graduates with a minimum BSEE or BSEET degrees. We not only pride ourselves on hiring students with strong technical backgrounds, but also with excellent communication skills. The ability to communicate your thoughts, ideas, and point of view is very important in this position and to the long-term development of your career. You must demonstrate the ability to work closely in teams and understand the dynamics of a team environment. We are looking for candidates that have demonstrated leadership skills and have the ability to be dynamic and persuasive in a professional setting. |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
9/4/2010
|
| R&D ASIC Engineer |
| Minimum Qualifications:
BS or MS in Electrical Engineering or Computer Engineering
? Exposure digital VLSI design
? Demonstrated Verilog/System-verilog design
? Knowledge of semiconductor devices and structures
? Understanding of physical implementation
? Understanding of analog design basics
? Understanding of digital ASIC design methods, tools and verification methodologies
? Understanding of physical VLSI ASIC design methods and tools
? Strong multi-tasking and teamwork skills
? Strong verbal and written communication skills
? Ability to understand systems and digital architectures
? Strong understanding of engineering mathematics |
| Agilent Technologies, Inc. US |
Santa Rosa |
CA |
9/4/2010
|
| New Product Manufacturing Engineer |
| Position requires
? BS/MS in Electrical/Electronic Engineering
? 3+ years Experience in the design or manufacturing engineering of RF and Microwave (MW) test instrumentation
? 3+ years Experience with New product Introduction (NPI) of RF and Microwave (MW) test instrumentation products
? Experience creating electrical product design or manufacturing test processes and technical documentation of these processes
? Experience with evaluation of new product designs to ensure manufacturability
? Sound knowledge of equipment calibration standards
? Experienced in setting manufacturing product specifications and statistically analyzing product performance
? Sound understanding of instrument measurement uncertainty analysis in accordance to stringent calibration lab requirements eg. ISO17025
? Programming in one or more of the following
o Unix, Linux, RMB, VB, C, C++, VEE, Labview, .NET (dotnet)
? Ability to interact effectively with people at all levels
? Strong knowledge of test instrument application & usage will be an added advantage
? Knowledge or experience in project management will be an added advantage |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Associate Engineer, R&D |
| List minimum education, training and experience needed to perform this job:
1. BSEE/BSET or 3 or more years of related experience.
2. Proficient in RF circuits a plus.
3. Knowledge of Network Analyzer, Signal Generator, Oscilloscopes, etc?
4. Experience with vacuum and cryogenic equipment a plus.
5. Proficient in Excel, MS Word and knowledge of Unix/Linux.
6. Domestic/ International travel; valid passport required. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Hardware Engineer-Cryogenics |
| List Minimum education, training and experience needed to perform this job:
1. BS Mechanical Engineering or related field
2. minimum 10 years experience with cryogenic and vacuum systems
3. fluent with CAD tools and thermal analysis programs
4. fluent with rf measurement tools including network analyzers, spectrum analyzers, noise figure, etc.
5. familiarity with NMR is a plus |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
9/4/2010
|
| Hardware Engineer-Materials Science |
| List Minimum education, training and experience needed to perform this job:
1. BS Materials Science or related field
2. minimum 3 years experience with cryogenic systems
3. fluent with CAD tools and thermal analysis programs
4. fluent with rf measurement tools including network analyzers, spectrum analyzers, noise figure, etc.
5. familiarity with NMR is a plus |
| Agilent Technologies, Inc. US |
Boulder |
CO |
9/4/2010
|
| API Process Development Scientist |
| Requires:
- BS/MS or PhD Chemistry, Biochemistry; or Life Science discipline or equivalent
- 3+ years hands on process development experience in pharmaceutical or biotechnology industrial
- Pharmaceutical pilot palnt experience desired
- Downstream and purification experience desirable
- Hands on experience with HPLC, GC-MS, LC-MS, MS-MS, NMR and other supporting analytical technologies for chemical synthesis
-Experience with DOE, statistical process control, Process Analytic Technology (PAT) applications and Quality by Design (QbD) initiatives desired
- A proven track record in product/process development of API's that have been successfully transferred validated and approved by the FDA or corresponding regulatory authority.
- Experience in development and successful transfer of safe, robust and scalable processes for the preparation of APIs.
- Knowledge of ICH Q7 and cGMP guidelines highly desired
- Excellent communication (oral and written), computer skills and interpersonal skills a must
- Ability to interface with global cross-functional internal and external customers and partners
- Track record of success in working with multiple projects in a fast pace environment managing to aggressive time lines and deliver projects on time
- Available for occasional business travel
Geo Location: Boulder, CO |
| Agilent Technologies, Inc. US |
Boulder |
CO |
9/4/2010
|
| North American Pharmaceutical API Sales |
| ? BS/MS in Chemistry or a Life Sciences discipline, or equivalent.
? 5+ years related direct sales experience selling Life Sciences products/services
? A demonstrated track record of successfully selling against a quota.
? High level of experience interacting with senior level customers from biopharma companies.
? Knowledge of drug development and CMC processes
? Working knowledge of competitive products (services, value propositions, price points).
? Demonstrated commercial selling skills. Strong business development and sales closing skills
? Effective interpersonal communication and telephone sales skills.
? Knowledge of DNA/RNA manufacturing and analysis technology highly desired
? Must be able to travel up to 50% of the time. |
| Agilent Technologies, Inc. US |
Cedar Creek |
TX |
9/4/2010
|
| Planner |
| You will need to be educated to at least university degree level and have at least 3 years' experience at a similar level. Your excellent organizational skills, vision and solutions-oriented approach are what will set your apart.
Geo location: Cedar Creek, TX |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Medicinal Chemist/ Research Scientist I |
| This position requires a MS in Synthetic or Medicinal Chemistry and at least 3 years experience as a medicinal chemist in an industrial setting with a proven record of achievement or a PhD and a post doc in Synthetic or Medicinal Chemistry.
Excellent communication skills are required, as the successful candidate will be expected to interact with scientists in other disciplines on a daily basis. Experience with Structure based design a plus.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Senior Clinical Staffing Consultant |
| ? 5+ years pharmaceutical clinical or medical recruiting experience a must, minimum of a Bachelors degree or equivalent
? Experience working in a fast-paced, highly matrix organization
? Proven track record of finding unique ways to source and attract qualified candidates
? Superior selection skills and a high level of proficiency in assessing individuals
? Proven ability cultivating successful relationships internally and externally
? Results driven, ability to demonstrate/quantify success relative to established targets and metrics
? Strong listening, facilitation and communications skills
? Strong organizational, multi-tasking and computer and web skills, along with the ability to handle sensitive and confidential situations/information
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Analytical Chemist, Scientist I |
| - A Ph.D. or Master's or Bachelor's degree in the life or physical sciences with a preference for a concentration in Chemistry, Analytical Chemistry or Pharmaceutical Chemistry
- 0 - 3 years (PhD), 3 - 5 years (MS) or 6+ years (BS) current relative industry experience working in drug substance and drug product support
- Scientist II: 3 - 5 years (PhD), 5+ years (MS) or 8+ years (BS) current relative industry experience working in drug substance and drug product support
- Broad understanding of the drug development process, including clinical design, chemical development, and formulation development, especially how those processes impact analytical method development, validation, and method transfer are essential
- High level understanding of risks in all aspects of method development, validation and transfer and the ability to use risk analysis and quality- by-design approaches to develop robust methods, design appropriate validation protocols to validate methods for their intended use, and ensure successful method transfer are essential
- Good understanding of ICH and FDA method validation guidelines are essential. The ability of identifying areas overlooked in the guidelines is preferred.
- Good understanding of GMP and hands-on GMP experience as well as how to develop methods that are GMP friendly are preferred.
- Skilled in HPLC, LC-MS, GC, GC-MS, FT-IR, UV-VIS, KF, NMR, dissolution and other instruments
- The ability to work successfully in both a team/matrix environment as well as independently
- The ability to work in a fast pace environment, manage priorities, and maintain timelines for multiple projects
- Excellent written and verbal communication skills
- Established organizational skills
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Principal Statistical Programmer |
| * B.S. in Biostatistics, Statistics, Computer Science, or a related field and a minimum of 10 years of SAS and relevant pharmaceutical industry experience
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Senior Medical Director, CF |
| · MD, DO or international equivalent
· Minimum of 5 years pharmaceutical industry experience, including time managing clinical trials and/or clinical development program(s)
· Preferred qualifications include sub-specialty training in internal medicine, family practice, pediatrics, pulmonary medicine, allergy, and/or industry background
· Board certification/eligibility in specialty area
· Ability to work collaboratively in a challenging team matrix environment
· Ability to work independently to resolve challenges and conflicts
· Possess a comprehensive understanding of applicable US and EU regulatory requirements and of the drug development process
· Have a working knowledge of biostatistics, data management, clinical operations and clinical pharmacokinetic scientific and technical processes
· Experience in filing and defending US INDs and/or NDAs
· Excellent communication skills
· Willing to re-locate to the Cambridge area
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Medical Director |
| ? MD, DO or international equivalent
? 2+ years of basic or clinical research experience in an academic setting with publications in peer reviewed journals
? 5+ years of experience in Clinical Development in the pharmaceutical industry
? Board certification in Internal Medicine, Infectious Disease or other relevant medical specialty
? Excellent communication skills
? Ability to work collaboratively in a team-based matrix management environment with minimal supervision
? Possess a full understanding of applicable US and EU regulations and of the drug development process
? Have a working knowledge of biostatistics and pharmacokinetics
? Experience in filing and defending US IND's or similar ex-US regulatory submissions
? Preferred qualifications include sub-specialty training in internal medicine, infectious disease (HCV), family practice, pediatrics, pulmonary medicine or allergy.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Associate Director, CLinical Pharmacology |
| * PharmD or Ph.D. and 5+ years of industry experience
* NCE drug development experience with at least 5 NCEs in the past
* Possesses good knowledge of drug Development Programs and a keen awareness of development issues
* Able to integrate the activities of distinct functional groups across multiple projects
* Can recognize and carry out productive new development initiatives/directions Is a mid-level experienced mentor who effectively infuses confidence and team commitment: can make clear written and oral presentations.
* Exhibits a record of excellent operational and ethical standards, and team-improvement
* Demonstrated ability to provide career development to staff
* Able to recognize and resolve important organizational problems and/or infusing innovation Has leadership abilities, can initiate and carry out tasks with little direct supervision
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Associate Medical Director |
| * MD, DO or equivalent ex-US medical degree (Non-MD candidates with doctoral degrees will be considered if they have an appropriate background in a clinical field)
* 1-2 years of basic or clinical research experience in an academic or industrial setting with experience in publications
* Clinical drug development experience and excellent communication skills
* Ability to work collaboratively in a team-based matrix environment and to function autonomously as appropriate
* Possess a full understanding of applicable US and EU drug development regulations and GCP regulations
* Have a working knowledge of biostatistics and pharmacokinetics
* Experience in interactions with regulatory authorities
* Willing to re-locate to the Cambridge area
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Manager, Health Value & Outcomes Research |
| Minimum Requirements:
? A bachelor?s degree in the life sciences, business administration or a related field with a preference for an advanced degree (MD, PharmD, MPH, MS, MHA or MBA). Educational focus in the areas of health economics or outcomes research would be beneficial
? 3 - 5 years of current experience with health economics and outcomes research for the biotechnology or pharmaceutical industries
? Working experience with economic modeling and payer market access tool creation
? Familiarity with payer dossiers, epidemiology, economic analyses, reimbursement and pricing environments
? A track record of success functioning in dynamic, matrix environments with the ability to multitask and adapt to rapid changes
? Exceptional written and verbal communication skills along with the ability to interact constructively across all levels of an organization and with thought leaders and other external collaborators
? The ability to effectively present technical data and complex concepts to diverse audiences
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Research Associate I |
| Experience working in a laboratory with skills in cell culture and standard molecular biology techniques (e.g., cloning and PCR) is required. Additional knowledge or experience in cell-based assays is desired. Meticulous attention to the details and regular maintenance of laboratory notebooks is required. The successful candidate must be a demonstrated team player and be able to work closely and responsively with their supervisor. Applicant must be able to follow appropriate biosafety procedures for working in an infectious disease laboratory.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Scientific Associate II |
| Minimum Education Requirements:
Bachelor?s degree in science or engineering field. Internship or undergraduate research project involving analytical laboratory work strongly preferred.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Associate Director/Director of Business Development |
| ? Medical or scientific education - a Masters degree at minimum, a PhD/MD degree is preferred.
? Relevant business experience (pharmaceutical, biotech, venture capital, investment banking, an MBA in addition will be favorably viewed).
? 3-5 years of business development experience; deal sheet demonstrating experience and past successes.
? Ability to forge relationships internally, as well as externally.
Skills / Competencies
? Able to work independently, as well as part of a team.
? Strong interpersonal skills, ability to persuade and motivate others.
? Ability to synthesize and summarize a complex set of facts and set opportunities within the broader strategic context.
? Adept at handling multiple projects and tight deadlines in a fast-paced environment.
? Strong project management, presentation and communications skills.
? Able to build and maintain contacts with potential partner companies
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Senior Formulation Development Scientist |
| - A degree in pharmaceutical sciences, chemistry, chemical engineering, materials science or related field
- PhD (or equivalent degree) and 4+ years of productive, relevant work or postdoctoral experience
- M.Sc. (or equivalent degree) and 7+ years of productive, relevant work experience.
- B.Sc. (or equivalent degree) and 10+ years of productive, relevant work experience.
- Proven ability to apply the principles of the basic sciences such as physical and organic chemistry, thermodynamics, and materials science, to formulation and process development, using a rational, scientific approach.
- Demonstrated ability to develop solutions to complex problems with creativity and innovation
- Formulation development experience on solid oral dosage forms is preferred, especially experience with small molecule NCEs and poorly soluble compounds
- Experience with a range of dosage forms, including liquids, solids and oral, iv formulations, controlled release and pediatric applications would be advantageous
- Expertise in process scale-up and optimization from laboratory scale to pilot scale and registration scale as well as familiarity with engineering scale-up principles, i.e., dimensional analysis.
- Experience applying statistical approaches in the design and analysis of experiments would be advantageous
- Experience working with and managing interactions with contract manufacturing vendors
- Inventive and innovative, self-starter who is comfortable and successful working in a multi-disciplinary team under defined timelines
- Proven teamwork, leadership and collaboration skills, with a demonstrated ability to interact and influence manage all levels of business
- Excellent verbal and written communication skills
- Demonstrated strategic planning, and organizational skills
- Supervisory experience would be a plus but not necessary
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Formulation Development Scientist II |
| A PhD or MS degree (educational concentrations in chemistry, pharmaceutics or engineering preferred)
?Pharmaceutical industry experience of 2-5 years for PhD and 5+ years for MS
?Experience working with small molecule new chemical entities (NCEs) and exposure to early phase formulation development activities
?Experience with a range of dosage forms, including liquids, solids and oral. Experience with IV formulations as well as formulation development for poorly soluble compounds would be advantageous
?Proven experience managing the scale-up and manufacturing of solid oral dosage forms
?Proven ability to apply the principles of the basic sciences, such as physical and organic chemistry, thermodynamics, and materials science, to preformulation and formulation development, using a rational, scientific approach.
?Experience applying statistical approaches in the design and analysis of experiments would be advantageous
?A history of success working in environments defined by innovation and initiative
?Ability to work effectively and comfortably in a multi-disciplinary team under defined timelines
?Excellent leadership, teamwork and organizational skills
?Solid verbal and written communication skills
?Supervisory experience would be a plus but not necessary
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Database Developer/Engineer |
| Desired Skills:
MySQL, Linux, bash,
Nice to have:
Perl, Python, ColdFusion, Java, TalenD, ETL
Experience in working in all phases of the development cycle.
Experience maintaining and developing high availability MySQL RDBMS with replication.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Research Scientist II |
| The ideal candidate for this position will be highly motivated and minimally have an MS degree with at least 10 years, or a PhD or DVM with at least 8 years of hands-on experience in using relevant general/safety pharmacology assays, such as cardiovascular telemetry or Langendorff heart perfusion.
Extensive understanding of cardiovascular pharmacology and physiology is required. Demonstrated independent thinking, trouble-shooting skills, and ability to analyze, interpret, and translate physiological function data is a must. Industry non-clinical research experience and experience with assessing drug-induced QT prolongation is preferred. Extensive knowledge of Data Sciences International/Ponemah (P3P and DataQuest), EMKA Technologies, or similar software packages is necessary. Ability to write basic programs using SAS software for data analysis and statistics is a plus.
The candidate must be able to work independently and in a matrix and function team environment. Strong written and oral communication skills are required, including excellent report writing and presentation skills. Study outsourcing and/or supervisory experiences are a plus.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Senior Director, Safety Operations |
| - M.D. or Masters /Doctorate level in life sciences or allied health fields preferred; Bachelor degree in life sciences or allied health fields required; 8+ years of direct Pharmacovigilance experience
- Solid knowledge of safety database operations and function
- Strong knowledge of Global Regulations, standards and best practices regarding safety processing and reporting, safety surveillance and pharmaceutical industry compliance activities in pre-marketing and post-marketing
-Strong operational skills as demonstrated by leading previous projects or functions and or equivalent in training and education in areas such as lean sigma or MBA
- Excellent verbal and written communication skills.
- Self-starter with proven ability to thrive in a fast-paced environment handling multiple simultaneous high priority tasks
- Successful track record of developing and mentoring staff
- Maintains high ethical standards, including a commitment to Vertex's values and behaviors
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Program Manager, Exploratory Development and Lab Solutions |
| Minimum Education Requirements:
? BS/BA in a Science Field ? Chemistry, Biology, etc..
? A degree or related experience in an Information Systems or Computer Science field is a plus
Minimum Experience Requirement:
? Previous experience working in a Pharmaceutical Research environment
? Minimum 5 years defining, implementing, and supporting Research, Discovery and Lab Systems.
? Minimum 5 years in a Project Management role or equivalent role
? Part of an IS team that has been responsible for developing a strong product pipeline
? Consulting experience in working with Research and Discovery or Clinical solutions a plus
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Associate Director, Phase IV Research |
| ? A bachelor?s degree in the life sciences, business administration or a related field. An advanced degree in health sciences is a plus.
? 3-5 years experience in conducting human clinical trials as part of investigator team and/or pharmaceutical sponsor.
? Familiarity with Good Clinical Practice (GCP) procedures and rules/regulations for conduct of human clinical trials.
? Understanding of the processes required for conduct of IND- and non-IND clinical research, including protocol development, IRB (or Ethics Committee) review, and safety reporting.
? A track record of success functioning in dynamic, matrix environments with the ability to multitask and adapt to rapid changes.
? Exceptional written and verbal communication skills along with the ability to interact constructively across all levels of an organization and with thought leaders and other external collaborators.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Manager, Health Value & Outcomes Research |
| ? A bachelor?s degree in the life sciences, business administration or a related field with a preference for an advanced degree (MD, PharmD, MPH, MS, MHA or MBA). Educational focus in the areas of health economics or outcomes research would be beneficial
? 3 - 5 years of current experience with health economics and outcomes research for the biotechnology or pharmaceutical industries
? Working experience with economic modeling and payer market access tool creation
? Familiarity with payer dossiers, epidemiology, economic analyses, reimbursement and pricing environments
? A track record of success functioning in dynamic, matrix environments with the ability to multitask and adapt to rapid changes
? Exceptional written and verbal communication skills along with the ability to interact constructively across all levels of an organization and with thought leaders and other external collaborators
? The ability to effectively present technical data and complex concepts to diverse audiences
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Head of Medicinal Chemistry |
| Possessing a Ph.D. in medicinal or synthetic chemistry, the Head of Medicinal Chemistry will most likely be currently leading a small to medium size chemistry domain in a large pharmaceutical or biotech company and will meet the following qualifications:
(a) Have a minimum of 10 years experience, as a member of a successful multidisciplinary R&D team in pharmaceutical drug discovery, with a demonstrated track record in the chemical design and synthesis, as well as biological characterization of drug candidates
(b) Have experience in successfully leading and managing a mid-size (minimally 15 scientists) group conducting drug discovery research, including leadership of strategic planning of chemical patent protection, construction and management of spending budgets for researchers.
(c) Possess an expert knowledge in the modern methods of synthetic and medicinal chemistry with proven ability to successfully and simultaneously conduct medicinal chemistry on multiple projects
(d) Possess a strong knowledge of computational chemistry methods and understanding of the target-based taxonomy of drug candidates as well as a solid working knowledge of biophysical methods such as: X-ray crystallography, macromolecular NMR, high-throughput screening as applied to drug discovery, and preferably how scale-up chemistry and formulations development are expedited for development candidates
(e) Command a solid grasp of cellular /molecular biology, biochemistry, disease pharmacology, mechanisms of drug metabolism and molecular toxicology, pharmaco-kinetic and pharmaco-dynamic sciences, and the evaluation of formulations for the in vivo evaluation of drug candidates
The Head of Medicinal Chemistry will be a dynamic and innovative scientist, with a well-developed sense of self-awareness, leadership and independence. Further, he or she will be an inspirational communicator, in written and verbal formats, with the demonstrated ability to instill vision for department, and collaborate effectively with counterparts in diverse domains such as biology, pharmacology, computational sciences and biophysics. As a vital part of Vertex? research management team, he or she will play a critical role in enabling the discovery goals of the research site.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Sr Scientist, DMPK |
| - Ph.D., or equivalent degree; Post Doctoral Experience is additional qualification.
- 6 - 10 years of Pharmaceutical Industry experience in DMPK
- Experience in GLP regulations, SOPs, interactions with Toxicology, Clinical Pharmacology, Clinical Research, Pharmaceutical Research and Development
- Demonstrated understanding of drug development process within different therapeutic areas
- Good verbal, writing and communication skills and project directed presentation skills
- Working knowledge of drug development process and ICH requirements for drug development
- Established supervisory and ability to operate in a matrix environment
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Scientist I |
| A Ph.D. or Master's or Bachelor's degree in the life or physical sciences with a preference for a concentration in Chemistry, Analytical Chemistry or Pharmaceutical Chemistry
- 0 - 3 years (PhD), 3 - 5 years (MS) or 6+ years (BS) current relative industry experience working in drug substance and drug product support
- Broad awareness of the drug development process, including clinical design, chemical development, and formulation development, especially how those processes impact analytical method development, validation, and method transfer are essential
- Good understanding of GMP and hands-on GMP experience as well as how to develop methods that are GMP friendly are preferred.
- Have received general training/coursework on analytical instruments;
- Working knowledge of analytical instrumentation such as HPLC, GC, UV-VIS, LC-MS, KF, and dissolution apparatus required.; experience with USP IV flow through apparatus a plus.
- Solid experience with HPLC-UV method development preferred.
- Strong capabilities with Excel or other spreadsheet based applications, statistically training a plus.
- The ability to work successfully in both a team/matrix environment as well as independently;
- Familiarity with various sold dosage forms: including tablets, capsules, and solid dispersions is desirable;
- The ability to work in a fast pace environment, manage priorities, and maintain timelines for multiple projects
- Excellent written and verbal communication skills, including familiarity with Scifinder and other journal databases
- Established organizational skills
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Manager, Research and Development Alliances |
| Minimum Education Requirements:
? BS/BA in a Science, Information Systems or Computer Science
Minimum Experience Requirement:
? Previous experience working in a Pharmaceutical Research and Development environment
? Minimum 7 years business analysis / project management and support of Research, Development and Lab Systems.
? Demonstrated Management Skills in a Research Or Clinical Environment.
? Part of an IS team that has been responsible for developing a strong product pipeline
? Consulting experience in working with Research and Discovery or Clinical solutions a plus
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Scientist I |
| Minimum requirements:
- A Ph.D. or Master's or Bachelor's degree in the life or physical sciences with a preference for a concentration in Chemistry, Analytical Chemistry or Pharmaceutical Chemistry
- 0 - 3 years (PhD), 3 - 5 years (MS) or 6+ years (BS) current relative industry experience working in drug substance and drug product support
- Broad awareness of the drug development process, including clinical design, chemical development, and formulation development, especially how those processes impact analytical method development, validation, and method transfer are essential
- Good understanding of ICH and FDA method validation guidelines are essential. The ability of identifying areas overlooked in the guidelines is preferred.
- Good understanding of GMP and hands-on GMP experience as well as how to develop methods that are GMP friendly are preferred.
- Working knowledge of analytical instrumentation such as HPLC, GC, UV-VIS, LC-MS, KF, and dissolution apparatus required.; experience with USP IV flow through apparatus a plus.
-Solid experience with HPLC-UV method development preferred.
- Strong capabilities with Excel or other spreadsheet based applications, statistically training a plus.
- The ability to work successfully in both a team/matrix environment as well as independently;
- Familiarity with various sold dosage forms: including tablets, capsules, and solid dispersions is desirable;
- The ability to work in a fast pace environment, manage priorities, and maintain timelines for multiple projects
- Excellent written and verbal communication skills, including familiarity with Scifinder and other journal databases
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Director, Health Value & Outcomes Research |
| ? Advanced degree (MD, PharmD, MPH, MS, MHA or MBA) and an educational or work experience focus in the areas of health economics and outcomes research.
? At least six years of health economics and outcomes research experience in the biotechnology or pharmaceutical industries, including experience with economic modeling, creating market access tools for payers, and managing cross-functional working teams
? Understanding the purpose, content/format, and utilization of AMCP and global value dossiers for formulary and/or reimbursement submission.
? Excellent knowledge of global pricing and reimbursement environment and the requirements of health technology assessment agencies.
? Demonstrated expertise in design and execution of outcomes research and economic analyses.
? Experience with assessment and utilization of available patient reported outcomes instruments in a variety of disease areas. Development and validation of PRO instruments a plus.
? Direct and successful interactions with regulatory authorities regarding PROs and outcomes research preferred.
? A track record of success functioning in a dynamic matrix environment with the ability to multitask and adapt to rapid changes seamlessly.
? Exceptional written and verbal communication skills along with the ability to interact constructively across all levels of an organization and with thought leaders and other external collaborators and customers.
? The ability to effectively present technical data and complex concepts to diverse audiences.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Clinical Outsourcing Manager |
| · Bachelor's degree is required
· Life sciences or business experience is preferred
· Minimum of 3 years experience in clinical development including knowledge of contract law and budgets
· Negotiation, organizational and communication skills are required
· Previous experience with clinical trial site agreements is a plus
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Sr. Director, Clinical Epidemiology |
| -M.D. or PhD. in Epidemiology required, as well as formal training in epidemiology
8+ years of pharmaceutical pharmacovigilance experience or equivalent in the field of clinical epidemiology
-Solid knowledge of general medicine and clinical practice evidenced by medical training and/or medical practice experience or designing/conducting clinical epidemiological trials.
-Highly evolved understanding of pharmacovigilance guidelines and regulations
-Effectively interacts with Senior Management and integrates activities successfully across the organization
-Excellent verbal and written communication skills
-Strong leadership skills and experience working in a matrix environment
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Safety Medical Director |
| M.D. required; 3+ years of
pharmaceutical pharmacovigilance experience, ideally both pre- and
post-marketing.
- Solid knowledge of general medicine and clinical practice, evidenced by
medical training and/or medical practice experience.
- Strong leadership skills, as well as experience working in a matrix
environment.
- Must have a strong working knowledge of FDA regulations/ICH guidelines
- Must be experienced in safety reviews of IBs, protocols, final clinical study
reports, and summaries of safety.
- Advanced ability to read, analyze and interpret clinical data and information
- Possess very strong writing skills and advanced verbal communication and
presentation skills.
- Requires strong attention to detail in writing and/or proofing materials
- Ability to work in a fast paced environment with demonstrated ability to
simultaneously manage multiple competing tasks and demands.
- Ability to work independently, take initiative and complete tasks to
deadlines.
- Occasional domestic and international travel may be required (
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Sr Scientist, Commercial Support, QbD and CMC |
| * Education and experience related to organic analytical chemistry (Ph.D. degree with three to five years experience or a Masters degree with ten years extensive pharmaceutical industry experience)
* At least 2 years of practical experience in analysis of small organic molecules with HPLC-MS
* Very good team-working skills and the capability to work in a complex environment
* Efficient organization and good documentation skills
* Good command of English; excellent presentation and report writing skills.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Director, Health Economics |
| - Bachelor?s degree in the sciences with a preference for a graduate level degree in a related field of study (e.g. PharmD, PhD, MD, MPH)
- Minimum of 6 years of relevant experience in health economics, and/or pricing functions
- 4+ years of managing or leading project teams is preferred, experience in developing and managing teams and working in cross functional environment is essential
- Health care industry experience and in-depth knowledge of the pharmaceutical business including R&D, clinical and marketing, as well as a good understanding of managed care;
Related therapeutic experience is preferred, specialty pharmacy category (e.g. HIV, MS, Oncology, etc.) experience considered a plus
- Experience in developing innovative communication strategies and tools to support brand and/or disease value propositions is essential. Experience in developing and/ or utilizing HE tools is preferred
- Excellent interpersonal skills are required as is the ability to understand and respond to multiple internal and external customer requests and manage conflict constructively with minimal supervisory support required
- Experience in preparing or reviewing materials for drug formularies considered a plus
- Ability to travel up to 20%
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Medical Information Specialist |
| * PharmD with on-the-job medical writing experience required
· One to two years experience in the pharmaceutical industry desired
· Ability to manage multiple assignment simultaneously, work independently
· Requires initiative and the ability to maintain a high level of productivity with minimal supervision
· Excellent ability in searching medical literature, interpret and present scientific/clinical trial data and understand statistical analyses
· Expertise in Microsoft Word is required
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Manager, Information & Records Management |
| * B.S. in Life Sciences or Library Science (or equivalent degree) and 5 ? 8 years of relevant work experience
* Prior experience as a manager and expertise in GCP/GLP documentation practices and 21 CFR Part 11
* EDMS / Documentum experience preferred
* Basic knowledge of global regulatory submission and clinical TMF documentation and demonstrate strong communication skills and be able to lead others in a changing environment
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Clinical Pharmacology Associate |
| * Bachelor?s degree in quantitative discipline or biological sciences with significant courses in quantitative area.
* Must have some programming skills (preferably in SAS/Splus).
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Clinical Safety Specialist |
| * B.S. (or equivalent degree) and 3 ? 5 years of relevant work experience, or
* PharmD, M.S.N (or equivalent degree) and 1 ? 4 years of relevant work experience
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Manager, Medical Coding, Clinical Data Management |
| * M.S. and 8+ year of relevant experience or a B.S. with 10+ years of relevant experience
* Must demonstrate relevant industry experience, with clear understanding of Medical Coding for Clinical data.
* Demonstrated track record of achieving results in related operations
* Proficiency with medical coding, reporting, and EDC tools, such as dsNavigator, Central Coding, InForm, J-Review
* Strong working knowledge of applicable regulations and industry trends
* Experience in demonstrating leadership, influence and collaboration in a matrix-managed environment
* Solid management experience and the ability to hire and develop staff, as well as leverage resources from within function
* Strong consultative, listening and analytical skills
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Senior Clinical Pharmacologist |
| * PharmD or Ph.D. and 2-5 years of industry experience
* NCE drug development experience with at least 5 NCEs in the past
* Possesses good knowledge of drug Development Programs and a keen awareness of development issues
* Able to integrate the activities of distinct functional groups across multiple projects
* Can recognize and carry out productive new development initiatives/directions Is a mid-level experienced mentor who effectively infuses confidence and team commitment: can make clear written and oral presentations.
* Exhibits a record of excellent operational and ethical standards, and team-improvement
* Demonstrated ability to provide career development to staff
* Able to recognize and resolve important organizational problems and/or infusing innovation Has leadership abilities, can initiate and carry out tasks with little direct supervision
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Manager, Global Trial Activation (GTAG) |
| * Experience and skills leading inter-departmental projects
* Proactively seeks out and recommends process improvements
* Proven track record of anticipating potential study start-up problems and preparing contingency plans as needed
* Communicates clearly and precisely with all levels of the company
* Demonstrated management skills for individual and team development.
* Understanding and experience with global regulatory environment, strong working knowledge of ICH/GCP guidelins; Bachelor?s degree required, advanced degree preferred, with 7+ years of relevant industry experience
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Sr. Statistical Programmer |
| Experienced with all SAS language, procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH.
Experienced with the CDISC SDTM and AdaM models and transforming raw data into these standards.
Experienced working with all types of safety data and coding dictionaries (MedDRA and WHODRL) commonly used by the pharmaceutical industry.
Experienced working in a team environment providing technical leadership and solving clinical trial reporting problems of moderate to high complexity within budget and customary time line constraints while assuring high quality standards.
Skilled at performing quality control checks of SAS code and output produced by other Statistical Programmers.
Knowledgeable regarding software validation and system development life cycle concepts.
B.S. in Biostatistics, Statistics, Computer Science, or a related field and a minimum of 5 years of SAS and relevant pharmaceutical industry experience.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Temp. Clinical Staffing Consultant |
| Minimum Requirements
· 5+ years pharmaceutical clinical or medical recruiting experience a must, minimum of a Bachelors degree or equivalent
· Experience working in a fast-paced, highly matrix organization
· Proven track record of finding unique ways to source and attract qualified candidates
· Superior selection skills and a high level of proficiency in assessing individuals
· Proven ability cultivating successful relationships internally and externally
· Results driven, ability to demonstrate/quantify success relative to established targets and metrics
· Strong listening, facilitation and communications skills
· Strong organizational, multi-tasking and computer and web skills, along with the ability to handle sensitive and confidential situations/information
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Director, Clinical Operations |
| * Global experience within all phases of drug development with advanced understanding of other functions; including but not limited to: Research, Non-Clinical, Supply Chain, Commercial, Regulatory and Medical Affairs
* Experience in strategic planning, business process improvement and achieving results.
* Experience in demonstrating leadership and influence and collaboration in a matrix environment
* Application of Project Management tools, methodologies, practices, risk analysis, decision analysis and contingency planning
* The ability to effectively communicate with Clinical Leadership and Clinical Project Managers
* Strong consultative, listening and analytical skills
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company?s strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex?s product pipeline is focused on viral diseases, inflammation, autoimmune diseases, cancer, pain and bacterial infection.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
9/4/2010
|
| Director, Clinical Site Services |
| * Bachelor?s degree required, advanced degree preferred ,with 7+ years of relevant industry experience
* Extensive experience strategizing and implementing global study execution activities
* Extensive experience strategizing and implementing global study execution activities
* Ability to thrive in a fast-paced, evolving environment with experience in a matrix organization
* Excellent verbal and written communication skills, superb oral presentation skills
* Ability to thrive in a fast-paced, evolving environment with experience in a matrix organization
* Solid working knowledge of ICH/GCP guidelines
* Successful track record managing direct reports and contractors
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain.
Vertex Pharmaceuticals |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Training Manager, Reclast |
| ? Bachelor?s degree
? Strong written, oral communication skills
? Extensive therapeutic experience,
? 3-4 years of pharmaceutical sales experience
? Strong clinical & Therapeutic knowledge
? Brand strategy, tactics understanding
? Partnering Skills (brand, medical, PRC, vendors etc)
? Presentation and platform skills. Ability to communicate in small and large settings
? Knowledge of field /sales force (key client knowledge)
? Administrative management skills - planning, organization, operational decision making and analysis.
? Creativity and innovation.
? Thorough knowledge of pharma industry, Novartis products and competition.
? Ability to manage multiple projects
? Fluent English (oral and written) |
| Novartis Oncology |
na |
CO |
9/4/2010
|
| Technical Services Scientist |
| ? BS degree required (Engineering or Pharmacy is preferred)
? 6 years related experience with BS Degree
?4 years related experience with MS Degree
? 2 years related experience with PhD Degree
Competencies:
?Technical Competence
? Solid Knowledge of cGMP and FDA regulations and guidelines
? Good Written and Verbal Communication Skills
?Speed/Action/Simplicity/Initiative |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Team Leader II, ARD |
| PhD, Chemistry or closely related scientific field, with 3-5 years of related pharmaceutical experience. MS, Chemistry or closely related scientific field, with 5-7 years related pharmaceutical experience. BS, Chemistry or closely related scientific field, with 7-10 years related pharmaceutical experience. Minimum of 2-4+ years previous and demonstrated supervisory experience. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Strategic Alliances Negotiator |
| Minimum requirements An Bachelor?s or Master?s Degree is a scientific area is desired, as is either an MBA or a JD, the Strategic Alliances Negotiator will possess an excellent in-depth
knowledge of the pharma/biotech arena, and will
have at least five years experience in a licensing or business development role. He or she will have a demonstrated capability for completing high quality transactions.
Experienced in partnering with biotechnology companies and/or academic/research institutions, he
or she will possess superior analytical, strategic and
communication skills. Well organized, detail oriented,
with a strong sense of urgency, the Negotiator will be a
team player comfortable working in a global matrix
system. A creative thinker, he or she will establish
innovative business solutions and concepts with a
strong strategic vision, consensus building talent,
negotiation skills, and a strong entrepreneurial spirit.
Considered reliable, pro-active, hands-on, able to
manage projects and function with autonomy, he or
she will understand how to influence people and
situations in an R&D setting. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Sr. Investigator, Global Imaging/MRI |
| The ideal candidate will have a PhD with a minimum of 2-4 years experience (although greater experience is deemed an asset) within industry/academia in the following areas:
- Small animal MRI experience (preferably on Bruker systems) may include multimodality imaging
- Extensive knowledge of imaging application
- Animal skills, such as handling, restraining, anesthesia and injections (IP, IM, IV) in rodents and rabbits.
- Proficiency in data analysis using Excel and statistical software, image processing; computer proficiency (e.g. C++, Matlab, IDL, Linux) is a plus.
- Good inter-personal, communication skills, and working with diverse and talented scientific teams. |
| Novartis Oncology |
na |
CA |
9/4/2010
|
| Sr. Auto & Controls Engineer |
| ? Requires a Bachelors degree in an engineering or related discipline. Equivalent experience may be accepted.
? Requires a minimum of 8 years industry work experience.
? Must be very comfortable with 21 CFR Part 11 and GAMP.
? Must have 5 years experience in a GMP pharmaceutical manufacturing environment or other regulated environment.
? Experience with computer-assisted engineering and design software, CAD and graphics skills are a plus.
? Batch processing and/or filling/packaging controls experience are a must.
? BMS experience is a plus.
? Must possess sound technical judgment and use structured decision-making techniques.
? Good oral and written communication skills are a must.
? Strong computer skills are required.
? Must have an ability to provide technical engineering support in a collaborative, team-oriented project environment.
? Strong project management skills are required.
? Project management skills are a plus. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Statistical Programmer |
| BA/BS or equivalent experience in mathematics, statistics, computer science or life sciences or related field,
- Fluent in English (oral and written)
Intermediate knowledge of and experience with SAS software.
- Working knowledge of database design/structures.
- Good understanding of global clinical trial practices, procedures, methodologies.
- Good understanding of regulatory requirements relevant to SR (e.g, GCP, ICH).
- Intermediate knowledge of office tools.
- At least 4 years experience in a programming role preferably supporting clinical trials and/or in the pharmaceutical industry (2 years for MS Statistics/Computer Science graduates). |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Sr Scientist, Protein & Toxicology Lab (non PhD role) |
| Minimum Requirements
? Education: Bachelor or Master Degree in Chemistry, Biochemistry, Physiology, Cell Biology, Toxicology or a related Biological Science, with 5+ years of academic or industrial experience in with significant experience in protein mass spectrometry.
? Extensive hands-on experience in the protein biochemistry methods, such as HPLC/Bioplex/gel electrophoresis/cell culture methods etc. Hands-on experience with peptide LC/MS/MS analysis is a great plus.
? Expertise in one or more of the following areas would be an advantage: protein detection assays; functional analysis of proteins in mammalian cells; purification of native and recombinant proteins; protein-protein and protein-ligand binding studies, knowledge of toxicology or cell biology
? Fluency in English (written and spoken).
? Flexibility and ability to work in a team, comfortable with multitasking, good written and oral communication skills, independent and accurate working style, ability to plan and organise effectively, willingness to take on additional responsibilities are expected. |
| Novartis Oncology |
na |
NE |
9/4/2010
|
| Sr Process Engineer |
| Required: BS degree in an appropriate scientific, pharmaceutical or engineering discipline and atleast 7 to 10 years of demonstrated experience in pharmaceutical formulation, packaging engineering, and/or process development. Experience with pharmaceutical production practices, manufacturing and packaging equipment, and instrumentation and controls. Working knowledge of GxPs. Demonstrated ability to execute facility, process, computerized system, cleaning, and equipment validations.
Preferred: Packaging Engineer or Electrical Engineer with advanced degree. Prior accomplishments in pharmaceutical formulation, development for various dosage forms, or packaging engineering in relevant environments. Prior experience executing capital projects. Working knowledge of analytical testing preferred; demonstrated experience with quality engineering methodology desired.
Only on-line resumes will be accepted. If you require accommodation under the American?s with Disabilities Act to apply for this position,contact Suzanne Drew at (402) 467-8808. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Principal Biostatistician |
| At least Masters Degree in Statistics (or equivalent degree) with 5 years of experience or PhD with 2-3 years of experience.
Fluent English (oral or written)
1. Experience in all tasks of a Trial Statistician.
2. Proven knowledge in Statistics and its applications to clinical trials.
3. Proven knowledge of drug development and HA guidelines. Background medical knowledge, preferably in relation to the specific therapeutic area.
4. Proven knowledge of statistical software packages.
5. Good communication and presentation skills.
6. Good team player. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Modeler |
| Master?s Degree in a modeling-related field with a minimum of 5 years of relevant experience, or Ph.D. with a minimum of 2 years of relevant experience, or equivalent degree/expertise. Detailed understanding of molecular & cellular biology, pharmacology, toxicology, physiology and pathophysiology, and/or pharmaceutical R&D process is desirable.
1. Experience in applying either biology, pharmacology or statistics modeling to drug R&D, and exposure to two applied areas out of three at least via collaboration on projects.
2. Good level of knowledge in one or several of the following modeling areas, and knowledge in others: learning algorithms, molecular pathways, biology, tissue effects, physiology and pathophysiology, PK/PD, statistics.
3. Basic-to-good knowledge of the drug R&D process, including clinical development; background medical knowledge and PK/PD knowledge.
4. In-depth knowledge of relevant software packages.
5. Good data exploration skills. Ability to understand heterogeneous data and communicate effectively with people from diverse scientific backgrounds in a multi-disciplinary organization.
6. Exceptional written and verbal communication skills including the ability to interact effectively with a multi-disciplinary team.
7. Good business ethics.
8. Innovative attitude; creative approach to model implementation; welcomes problems as challenges; able to approach problems from multiple angles.
9. Well-developed organizational skills; good project management skills. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Mgr/Assoc Director Product Training |
| ? Bachelor's Degree required
? A minimum of three years of pharmaceutical sales experience required
? 2+ years pharmaceutical training experience strongly preferred
? Oncology experience preferred |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Medical Scientific Expert MD(Thrombosis) |
| Strong medical science components to clinical trials/program resulting in high quality analysis of data which enables strategic decisions within the clinical program.
Novartis seen as a credible, ethical and preferred partner by key investigators in the assigned TA.
Education:
? MD with unique knowledge for successful clinical program development and execution, with ? 3 years of clinical research experience required.
Or
? MD with specialty with board certification or equivalent required.
Languages:
Fluent English (oral and written)
Experience:
? Advanced medical/scientific writing and communication skills.
? Proven ability to interpret, discuss and represent efficacy and safety data relating to the assigned area.
? Proven ability to work both independently or in a cross functional team setting, including a matrix environment.
? Demonstrated ability to establish effective working relationship with key investigators in assigned TA.
? Medical and/or scientific expertise within a disease area preferred. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Medical Scientific Expert MD(Thrombosis) |
| MD with unique knowledge for successful clinical program development and execution, with ? 3 years of clinical research experience required.
Or
? MD with specialty with board certification or equivalent required.
Languages:
Fluent English (oral and written)
Experience:
? Advanced medical/scientific writing and communication skills.
? Proven ability to interpret, discuss and represent efficacy and safety data relating to the assigned area.
? Proven ability to work both independently or in a cross functional team setting, including a matrix environment.
? Demonstrated ability to establish effective working relationship with key investigators in assigned TA.
? Medical and/or scientific expertise within a disease area preferred. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Medical Scientific Expert MD(Metabolism) |
| ? MD with unique knowledge for successful clinical program development and execution, with ? 3 years of clinical research experience required.
Or
? MD with specialty with board certification or equivalent required.
Languages:
Fluent English (oral and written)
Experience:
? Advanced medical/scientific writing and communication skills.
? Proven ability to interpret, discuss and represent efficacy and safety data relating to the assigned area.
? Proven ability to work both independently or in a cross functional team setting, including a matrix environment.
? Demonstrated ability to establish effective working relationship with key investigators in assigned TA.
? Medical and/or scientific expertise within a disease area preferred. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Medical Dir/Executive Medical Director US Medical (Respiratory) |
| An MD, Ph.D., or PharmD (MD is preferred) with a minimum of 2-3 years of Pharmaceutical or equivalent experience, some experience working in US Medcial Affairs, Clinical Research experience related to Respiratory (Allergy Research is ok but less desirable), and in leading other Medical Directors in a Pharmaceutical or equivalent environment is required.
-Ability to orchestrate and synthesize situational analyses (i.e. evidence gap analysis, customer insights, trends in therapy, etc.) across a disease area portfolio of brands to aid in the development of the disease area strategy.
-Integration of portfolio customer & stakeholder strategies with portfolio medical strategies and business drivers.
-Ability to lead in a matrixed environment and influence internal partners to achieve desired business outcomes.
-Ability to communicate effectively, manage issues, resolve conflicts, and mitigate risks.
-Prior strategic leadership experience in pharma or biotech industry.
- Prior line management experience required (3-5 years is preferred).
- Proven proficiency in stakeholder management.
-Proven leadership in clinical strategy development, trial methods, and operations.
-Experienced in presenting scientific data both verbal and written.
-Team building skills
-Understanding of the US market and the stakeholders influencing decisions.
-Advanced business and market knowledge required. Understanding of international regulations applicable to clinical development.
-Basic understanding of biostatistics p values regression correlation Statistical analysis.
-Ability to travel up to 20-25% (some Global) |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Med Scient Expert nonMD |
| MD or PhD with unique knowledge for successful clinical
program development and execution, with 3-5 years of
clinical research experience required.
- Fluent English (oral and written)
- Advanced medical/scientific writing and communication
skills
? Proven ability to interpret, discuss and represent
efficacy
and safety data relating to the assigned area.
? Proven ability to work both independently or in a cross
functional team setting, including a matrix environment.
? Demonstrated ability to establish strong scientific
partnership with key investigators in assigned TA.
? Medical and/or scientific expertise within a disease area
required; Respiratory expertise preferred |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Sr Biostatistician |
| Education (minimum/desirable): At least Masters Degree in Statistics (or equivalent degree) with 7 years of experience or PhD with 4 years of experience.
Languages: Fluent English (oral and written).
Experience/Professional requirements:
1. Experience gained in the main tasks of program statistician (about 2-4 years).
2. Proven knowledge and expertise in statistics and its applications to clinical trials in at least one TA. Solid experience in drug development process and HA guidelines
3. Background medical knowledge, preferably in relation to the specific therapeutic area.
4..Good knowledge of statistical software packages.
5. Very good project management skills.
6. Very good communication and presentation skills.
7. Ability to give effective guidance to Trial Statisticians and Program Programmers.
8. Good team player. Good business ethics.
9. Good leadership skills. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Small Molecule NMR Scientist (B.S./ M.S.) |
| M.S. or equivalent with 0-5 years or more relevant experience in small molecular NMR with demonstrated success in modern NMR methodologies. Demonstrated skills in data collection and process, spectral interpretation, data management and instrument maintenance are essential. A background in organic chemistry and a keen interest to champion NMR based collaborative research projects with medicinal chemists are required. Proficiency in UNIX/LINUX and expertise in hyphenated NMR technologies are desirable. Excellent communication skills and the ability to multitask in a fast-paced environment are essential. A self-motivated individual as well as a strong team player is required. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Small Molecule Mass Spectrometry Lab Head |
| A Ph.D. scientist with 5+ years of relevant experience or an MS scientist with 10+ years of experience in small molecules MS, structure determination and open access LCMS. In-depth knowledge of mass spectrometry and related techniques and how these can be applied for the analysis of small organic molecules. Expertise in liquid and gas chromatography is expected. Expertise in automation is a plus. Excellent communication skills and the ability to multitask in a fast-paced environment are essential. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| siRNA Chemistry Associate Scientist (BS/MS) |
| ? BS or MS degree in chemistry
? 5+ years of experience in medicinal or
synthetic chemistry
? Is a creative, flexible, open minded, and
curiosity-driven scientist
? Has the ability to work effectively both
independently and with a multidisciplinary
team of medicinal chemists, biologists,
pharmacologists, engineers, and external
collaborators
? Flexibility to work in a fast-paced,
dynamic environment
? Has excellent oral / written
communication and presentation skills |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior Statistician Shanghai Chin |
| ?At least Master?s Degree in statistics or a closely related field.
?At least 5 years of experience in drug development (maybe acquired at a CRO) or a related area (2 years for Ph.D.).
?Proven knowledge of drug development and Health Authority guidelines.
?Good command of English, written and spoken.
?Ability to coordinate and oversee a team effort and to give effective guidance to programmers and to less experienced statisticians.
?Work or college experience in another country or demonstrated ability working together in a multicultural organization would be ideal.
?Advanced knowledge of statistical software, in particular SAS. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Senior Software Engineer (BS/MS) |
| The successful candidate will have a Master?s degree in computer science or equivalent experience. Along with a proven track record of building multi-tier, database-backed web applications the candidate should possess:
?Excellent interpersonal and communication skills
?Expert object-oriented programming and Java skills
?Experience with rapid development frameworks such as JBoss Seam
?Experience with Oracle, SQL, PL/SQL, and database design
?Expertise with web application servers
?Experience with Perl, C++, or languages in addition to Java
?Knowledge of Use Case design and UML
?Knowledge of service oriented architectures
?Experience handling ?omix data, especially MS based proteomics data
?At least six years of industry experience preferred |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior Scientist-Analytical |
| Education:
Minimum: BS/MS or equivalent experience.
Desirable: Advanced degree in a scientific or relevant discipline (Ph.D. or equivalent).
Languages: Fluent English (oral and written)
Experience/Professional Requirement:
1. Minimum of 3 successful years of experience as scientist (promotional pathway) or Ph.D. (0 years experience) or equivalent.
2. Awareness/proven experience for safe handling of chemicals, potentially dangerous materials and equipment.
3. Broad scientific or technical knowledge in a specific area (e.g. synthetic, analytical or galenical).
4. Adequate understanding of development processes.
5. Advanced knowledge in scientific/technical areas of collaboration.
6. Advanced knowledge of laboratory and/or technical tools.
7. Good knowledge of software and computer tools.
8. Good presentation skills and scientific/technical writing skills. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior Scientist-Analytical |
| Education:
Minimum: BS/MS or equivalent experience.
Desirable: Advanced degree in a scientific or relevant discipline (Ph.D. or equivalent).
Languages: Fluent English (oral and written)
Experience/Professional Requirement:
1. Minimum of 3 successful years of experience as scientist (promotional pathway) or Ph.D. (0 years experience) or equivalent.
2. Awareness/proven experience for safe handling of chemicals, potentially dangerous materials and equipment.
3. Broad scientific or technical knowledge in a specific area (e.g. synthetic, analytical or galenical).
4. Adequate understanding of development processes.
5. Advanced knowledge in scientific/technical areas of collaboration.
6. Advanced knowledge of laboratory and/or technical tools.
7. Good knowledge of software and computer tools.
8. Good presentation skills and scientific/technical writing skills. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Senior PhD Scientist: Protein Purification and Expression |
| The Lab Leader of protein expression and purification group will possess the following qualifications:
?PhD with a minimum of five years of research in protein expression, purification, biochemistry or closely related discipline.
?General knowledge of state-of-the art technologies, platforms and approaches which enable practical yet innovative ways to support drug discovery programs.
?Thorough understanding of protein chemistry, biochemistry, bacterial, yeast and mammalian expression systems for tool generation to ensure the success of target-driven drug discovery.
?Strong command of academic or commercial research efforts and of scientific literature, and knowledge of key opinion leaders in the area.
The Leader of protein group will be a decisive and results-oriented individual who is flexible, team-oriented, creative and able to excel in a multi-project, fast-track environment. He or she will be a strategic thinker who interacts and collaborates with project teams, peers and management in identifying and achieving discovery goals from both scientific and strategic perspectives. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior Investigator, Clinical PK/PD |
| Ph.D./Pharm.D. level scientist with 3 years of relevant experience, or Masters Level with at least 5 years relevant experience.
At least 3 years experience in drug development or a relevant environment (e.g. Clinical Pharmacology or Drug Metabolism and Pharmacokinetics).
Proven knowledge of PK and PK/PD evaluation techniques.
Experience of working in project teams (preferably global) and sound awareness of recent developments in drug development sciences essential.
Knowledge of regulatory requirements and experience in dealing with regulatory authorities. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior Investigator, Clinical PK/PD |
| Minimum Requirements:
Ph.D./Pharm.D. level scientist with 3 years of relevant experience, or Masters Level with at least 5 years relevant experience.
At least 3 years experience in drug development or a relevant environment (e.g. Clinical Pharmacology or Drug Metabolism and Pharmacokinetics).
Proven knowledge of PK and PK/PD evaluation techniques.
Experience of working in project teams (preferably global) and sound awareness of recent developments in drug development sciences essential.
Knowledge of regulatory requirements and experience in dealing with regulatory authorities. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior Data Manager |
| Education: Bachelors degree in life sciences, computer science, pharmacy, nursing or equivalent relevant degrees.
Languages: Fluent English (oral and written)
Experience/ Professional Requirements:
1) Ideally 5 or more years experience in drug development with at least 4 years in Data Management activities.
2) Project team leadership experience required.
3) Good technical and problem solving skills.
4) Thorough understanding of clinical trial methodology GCP and medical technology.
5) Ability to work independently, under pressure demonstrating initiative and flexibility.
6) Attention to detail and quality focused.
7) Good organization planning and project management skills.
8) Good interpersonal and communication skills and ability to operate effectively in an international environment.
9) Good negotiation skills.
10) Thorough understanding of physiology, pharmacology, clinical study objectives and the drug development process.
11) Ability to mentor, coach within Data Management and cross functionally and train internal and external partners. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Senior Business Analyst, Bioinformatics |
| Qualifications:
? Idea candidate should have an advanced degree in biology and/or B.S in Computer Science
? At least 3-5 years experience in a scientific or biotech environment
? Strong communications and interpersonal skills
? Proven capabilities interacting with scientists and being customer service oriented
? Ability to work independently and/or as part of a team
? Extensive knowledge in the biology, working experience related to the drug metabolism and pharmacokinetics research process will be strong plus
? Good understanding and practical experience in data management and data analysis tools to support research process
? Solid understanding of relational databases and familiarity with Oracle and/or SQL server
? Strong software engineer knowledge and extensive practical experience |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Senior / p-CRF Developer |
| BA/BS in life science, computer science, pharmacy, nursing or equivalent.
Fluent English (oral and written).
1. 2-5 years working experience in software based paper forms design
2. University degree in Life Sciences, Mathematics, Computer Science, Medical Informatics or equiva-lent degree
3. Solid knowledge of medical terminology.
4. Exposure to knowledge of Clinical Research prac-tices and procedures, stages of clinical trials, drug development process, requirements and guidelines for data collection.
5. Solid knowledge of the software used with pCRF design in EDM, specifically the electronic publishing system for pCRF production.
6. Solid communication skills in order to be able to work with a wide variety of customers both face-to-face and via phone or e-mail. Requirement for excel-lent ENGLISH.
7. Exposure to ICH and Health Authority guidelines and regulations as they pertain to clinical database management and computer systems |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Scientist, Translational Safety Biomarker Lab |
| Educational requirements:
BS/MS degree in Biochemistry or Molecular
and/or Cell Biology, Biomedical engineering,
or related fields.
Experience:
5 or more years of practical experience in
assay, reagent, and technology development
in the life sciences industry. The successful
candidate will have experience in molecular
and/or chemical approaches to affinity-
reagent generation. It would be beneficial to
have experience working with biomarker
development, exposure to in vivo studies
both preclinical and/or clinical. The
preferred candidate will have expertise in
data summarization and analysis, oral and
written communication skills. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Scientist-Analytical |
| Education
Minimum: BS or equivalent experience.
Desirable: MS or equivalent.
Languages: Fluent English (oral and written)
Experience/Professional requirement:
1. Minimum of 3 successful years of experience as associate scientist (promotional pathway) or 3-5 year's (for BS) or 1-3 year's (for MS).
2. Awareness/proven experience for safe handling of chemicals, potentially dangerous materials and equipment.
3. Good scientific or technical knowledge in a specific area (e.g. synthetic, analytica or galenical).
4. Adequate knowledge in scientific/technical areas of collaboration.
5. Proficient with laboratory and/or technical tools.
6. Adequate knowledge of software and computer tools.
7. Basic presentation skills and scientific/technical writing skills. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Scientist I - Molecular Toxicology |
| Minimum Requirements
Technical Skill Sets:
? Demonstrated competence in performing a variety of molecular biology techniques (e.g. nucleic acid purification, cloning, TaqMan and SYBR green qPCR, siRNA/shRNA knockdown, etc?)
? Proficiency in isolating and cultivating cells from different organs in different species
? Demonstrated competence in performing a variety of biochemical techniques (e.g., preparation of cell and tissue extracts, subcellular fractionation, enzyme assays, protein detection assays (Western blotting, ELISA, Luminex, MSD?))
? Extensive experience with preclinical animal models, including animal handling, study design and protocol implementation, IV and oral dosing, and necropsy procedures
? Good understanding of SOPs as well as their practical implementation
? Fluency in English
? Working knowledge of relevant IT systems and software
Experience:
? At least 5 years of experience in cellular/molecular biology and/or toxicology in academic and/or industrial environment
? Excellent knowledge of mammalian cell culture models (primary cultures and cell lines) and related techniques
? Excellent knowledge of molecular & biochemical analytical techniques
Personal Skill Sets:
? Interpersonal and teamwork skills
? Independent and proactive work ethic
? Outstanding oral communication and writing skills
? Computer skills for experimental organization, assay design, data collection and analysis, and report writing
Education:
Bachelor?s or Master?s degree in life sciences, preferably molecular biology, biochemistry, cell biology, or molecular toxicology |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Scientist I |
| Education & Experience
BS, MS, or PhD, Chemistry, or other scientifically related field. BS degree + 5 or MS +3 years experience as an analytical chemist or MS, Chemistry with 2+ years experience within method development. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Scientist I |
| Bachelor?s Degree in analytical chemistry or a related discipline plus at least 5 years (or M.S. and 3 years) of relevant experience in quantitative analytical techniques involving the automated extraction and analysis of small and/or large molecules in biological samples using LC-MS/MS. Experience in a GLP laboratory environment, proficiency with personal computer applications for word processing, spreadsheets and graphics, as well as good oral and written communication skills are desirable. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Scientific Associate: Oncology Biotherapeutics |
| Candidates should possess a BS/MS degree with 2-5 years of relevant laboratory experience. Candidates who have worked in the Pharma/ Biotech industries are particularly encouraged to apply. Knowledge of cell signaling pathways as related to oncology or other proliferative diseases is crucial. It is essential that you have an excellent working knowledge and direct experience of a breadth of cellular and molecular biological methods (especially RNAi, RT-qPCR, cloning, cell culture, transient/ stable cell line generation, immuno-detection, ELISAs and phenotypic characterization). You should be a scientifically motivated self starter, capable of independently conceiving, conducting and critically analyzing your own innovative experiments. Strong presentation skills, communication and the ability to work in a fast-paced team-oriented environment will also be vital. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Safety Toxicologist |
| ? BS or MSc degree and major in physiology, pharmacology, biomedical engineering or related field.
? Prefer 5 ? 10 years experience in cardiovascular physiology and/or pharmacology research.
? Prefer minimum of 2 years experiences in cardiovascular safety pharmacology research.
? Experience in setting up, conducting and reporting of telemetry studies in dog and monkey.
? Familiar with EMKA jacket system or other external jacket telemetry system and have experience in EMKA ECGAuto computer software (or similar computer software) to analyze cardiovascular telemetry data.
? Experience in using Excel and SAS macro to analyze and report cardiovascular parameters in telemetry.
? Experience in ECG analyses including ECG interval measurements and waveform abnormalities screening in dog and monkey. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Research Scientist: Biochemistry and Affinity Proteomics (BS/MS) |
| Candidates should have a BS or MS in Biochemistry or Biological Science with 3-8 years academic and/or industry experience. They must be well-versed in all aspects of protein purification including sample preparation, chromatographic and gel-based separations, electrophoresis, and cell culture. They should have experience in the design and implementation of biochemical assays and in data analysis. The ideal candidate is an independent worker, a self-starter, good at trouble shooting and thriving in a multidisciplinary environment. Excellent communication skills are required and a premium is placed on candidates with a track record of creativity and innovation.
Additional Experience:
Experience with activity-based probes, photoaffinity crosslinkers, sub-cellular fractionation, basic molecular biology techniques, and sample preparation for mass spectrometry is a plus. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Research Investigator, Preclinical Imaging, Investigative Toxicology |
| ? Ph.D. degree in Biochemistry, Physiology, Pharmacology, Toxicology, Biophysics, Biomedical Engineering or related field in the biomedical sciences
? At least 2 years of prior experience in pharmaceutical drug development and/or toxicological sciences required.
? Experience with hands-on in vivo small animal imaging, preferably with multiple imaging modalities. A strong expertise in small animal (rat, mouse) Ultrasound imaging for various applications including contrast enhanced ultrasonography is preferred.
? Expertise and knowledge in vascular toxcology and in vitro vascular ring assay would be a plus.
? Experience of managing highly skilled technical staff, laboratory equipment, consumables and safety is desirable.
? Fluency in English (written and spoken) is a must
? Flexibility and ability to work in a team, comfortable with multitasking, excellent interpersonal skills to communicate and collaborate within a multi-disciplinary environment, willingness to take on additional responsibilities are expected
? Excellent project management skills
Technical Skill Requirements:
? Experience with pre-clinical applications of MR imaging and spectroscopy, X-ray microCT, ultrasound and/or optical imaging
? Imaging data processing and analysis |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Research Associate, Molecular Imaging, PET/SPECT/CT |
| The ideal candidate will have a BS/MS in Biology, Biochemistry, Animal Sciences, Bioengineering, Biophysics or related field, and 3+ years of hands-on experience with PET/SPECT/CT imaging is a requirement, ideally in a drug discovery environment. Good organizational, interpersonal skills, and excellent communication and presentation skills are desirable.
Skills required: Technical proficiency in all aspects related to PET and extensive hands-on experience with small animal handling (including tail vein injection, catheter placement, perfusion, microdissection), and in vivo pharmacology. Strong computer/computational skills in data analysis. Creativity and the ability to work independently. |
| Novartis Oncology |
na |
SC |
9/4/2010
|
| Regl Scientific Mgr/Dir--Primary Care (North Carolina/South Carolina) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible.
Ability to travel approximately 60%. |
| Novartis Oncology |
na |
CA |
9/4/2010
|
| Regl Scientific Mgr/Dir Southwest OU--Respiratory (Northern CA) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Respiratory Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
MO |
9/4/2010
|
| Regl Scientific Mgr/Dir Southwest OU--Respiratory (AR, KS, and MO) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Respiratory Therapeutic Area and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Regl Scientific Mgr/Dir Southeast OU--IDTI (AL, FL, GA) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Infectious Diseases, Transplantation and Immunology Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
NE |
9/4/2010
|
| Regl Scientific Mgr/Dir NW OU--Primary Care (IA and NE) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Cardiovascular, Endocrinology, and Rheumatology Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
WA |
9/4/2010
|
| Regl Scientific Mgr/Dir NW OU--Primary Care (AK and WA) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Cardiovascular, Endocrinology, and Rheumatology Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
UT |
9/4/2010
|
| Regl Scientific Mgr/Dir NW OU--Multiple Sclerosis (CO, IA, NE, UT) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Multiple Sclerosis or Related Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
PA |
9/4/2010
|
| Regl Scientific Mgr/Dir NE OU--Multiple Sclerosis (Phila/Southcent PA) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Mutiple Sclerosis or Related Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
NY |
9/4/2010
|
| Regl Scientific Mgr/Dir NE OU--Multiple Sclerosis (New York City) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 2 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare environment to provide strategic and scientific/medical direction to national/regional business unit functions. Teaching experience preferred. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Business Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Previous experience within the Multiple Sclerosis or related Therapeutic Areas and/or in a Field-based position is a definite asset. Salary flexible. |
| Novartis Oncology |
na |
AZ |
9/4/2010
|
| Regl Scientific Mgr/AD, Hematology MSL, Southwest US |
| Position will be filled at level commensurate with experience. Advanced scientific degree (MD, PhD, or PharmD highly preferred) or oncology nurse with advanced degree required. Minimum of 5 years Oncology experience with a strong current working knowledge of Oncology required. Teaching experience preferred. Previous pharmaceutical industry experience preferred. Thought leader development experience is a plus. Knowledge of treatment guidelines, clinical research processes, FDA regulations and OIG guidelines is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important external customers, including medical thought leaders, academic institutions, large group practices, medical directors and pharmacy directors is required. Must be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society (ies) is a plus. Must be a strong team player who can effectively interface cross-functionally with Novartis clinical and commercial personnel. Working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel) and associated hardware is required. The position is associated with approximately 65% travel. |
| Novartis Oncology |
na |
PR |
9/4/2010
|
| Regional Medical Associate Director/Director (Puerto Rico) |
| The candidate must be locally based in Puerto Rico.
Position will be filled at level commensurate with experience:
Advanced scientific degree (M.D., Ph.D., or PharmD; M.D. is preferred). A minimum of 3 years of Postdoctoral experience in pharmaceutical industry (preferred) or other healthcare/managed markets environment.
Excellent interpersonal and oral and written communication skills in both English and Spanish are required.
Field based medical and/or managed care with teaching experience preferred.
Thorough knowledge of clinical medicine, managed markets, pharmacoeconomics, disease management, medical research and health policy in Puerto Rico are required.
Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations and ethical guidelines applied to the pharmaceutical industry preferred. Excellent presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, pharmacy directors and government officials is required. Must be science-oriented and be able to prioritize work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer?s unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, Powerpoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Operating Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RMAD/D position is associated with approximately 60% travel. Salary flexible. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| R&D Quality Engineer |
| Education Requirements:
Bachelor of Science degree in Reliability, Quality, Mechanical, Electrical Engineering, Math, Physics or equivalent.
Experience Requirements:
Minimum 5 to 10 years experience in Reliability engineering and testing. Medical Device experience preferred.
Ability to interpret, analyze, and present technical information using practical judgement.
Capable of functioning effectively in a team environment.
Proficient in Excel pivot tables and charting.
Excellent written and oral communication skills.
Demonstrated problem solving skills.
Ability to organize and manage concurrent activities.
Knowledge of advanced data gathering and analysis techniques, including statistical analysis.
Knowledge of standard quality and reliability tools such as FMEA (Failure Modes Effect Analysis), Root Cause Analysis, DOE and Statistics.
Proven ability to communicate effectively and manage relationships at all levels of the organization as well as cross-functionally to achieve reliability goal.
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| R&D Quality Engineer |
| Education Requirements:
Bachelor of Science degree in Reliability, Quality, Mechanical, Electrical Engineering, Math, Physics or equivalent.
Experience Requirements:
Minimum 5 to 10 years experience in Reliability engineering and testing. Medical Device experience preferred.
Ability to interpret, analyze, and present technical information using practical judgement.
Capable of functioning effectively in a team environment.
Proficient in Excel pivot tables and charting.
Excellent written and oral communication skills.
Demonstrated problem solving skills.
Ability to organize and manage concurrent activities.
Knowledge of advanced data gathering and analysis techniques, including statistical analysis.
Knowledge of standard quality and reliability tools such as FMEA (Failure Modes Effect Analysis), Root Cause Analysis, DOE and Statistics.
Proven ability to communicate effectively and manage relationships at all levels of the organization as well as cross-functionally to achieve reliability goal.
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| PTM (Project Team Member), Strategic Marketing, GPS |
| University degree in Medicine, Biological or Pharmaceutical Sciences. An advanced degree in bioscience, and/or business is a plus (e.g., MD, Pharm. D., PhD., MBA)
Strong science and business background
? Excellent understanding of Oncology market
? Extensive contact with Oncology/Hematology Medical experts
? Proven ability to operate and influence cross-functionally and cross culturally
? Proven leadership ability
? Strong analytical and strategic thinking skills
? Oncology product development experience
? Significant experience in launching new products |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Proteomics and Mass Spectrometry Scientist (BS/MS) |
| BS/MS in biology or chemistry with >5 years experience in a mass spectrometry laboratory. In-depth knowledge and hands-on experience with LC/MSMS and ESI of proteins and peptides. Excellent communication skills and the ability to multitask in a fast-paced environment are essential.
Experience in cell biology or cell culture is a plus. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Protein Biochemistry Research Associate (BS/MS) |
| B.S/M.S or equivalent in biochemistry or a related discipline with at least 2-3 years of research laboratory experience. A strong background in protein expression and purification is highly desirable. PhD level scientists should not apply.
The successful candidate will be expected to be able to participate in experimental design and to independently conduct experiments. They must also be detail oriented and be able to handle multiple tasks efficiently. The candidate must possess good communication skills and be comfortable working in a matrix based team environment. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Protein Biochemistry Research Associate (BS/MS) |
| B.S/M.S or equivalent in biochemistry or a related discipline with at least 5 years of research laboratory experience. A strong background in protein expression and purification is highly desirable.
The successful candidate will be expected to be able to participate in experimental design and to independently conduct experiments. They must also be detail oriented and be able to handle multiple tasks efficiently. The candidate must possess good communication skills and be comfortable working in a matrix based team environment. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Program Section Leader (MD) Thrombosis |
| Education (minimum/desirable):
MD, required
Advanced knowledge in medical/scientific area required.
Languages:
Fluent oral and written English.
Experience/Professional requirement:
? ?8 years of involvement in drug development spanning clinical activities in Phases II/IV or comparable experience in industry.
? ?4 years of demonstrated leadership and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing), or section of clinical programs in a global/matrix environment (including remote) in pharmaceutical industry.
? ?4 years people management experience required, this may include management in a matrix environment. Global people management experience desirable.
? Strong management, interpersonal, communication, negotiation and problem solving skills.
? Considerable organization awareness (e.g., inter-relationship of departments, business priorities), including significant experience working cross-functionally and in global teams.
? Medical/scientific and operational expertise appropriate to the program. |
| Novartis Oncology |
na |
NE |
9/4/2010
|
| Process Engineer |
| Required: BS degree in an appropriate scientific, pharmaceutical or engineering discipline and 3 to 5 years of demonstrated experience in pharmaceutical formulation, packaging engineering, and/or process development. Experience with pharmaceutical production practices, manufacturing and packaging equipment, and instrumentation and controls. Working knowledge of GxPs. Demonstrated ability to execute facility, process, computerized system, cleaning, and equipment validations.
Preferred: Packaging Engineer or Electrical Engineer with advanced degree. Prior accomplishments in pharmaceutical formulation, development for various dosage forms, or packaging engineering in relevant environments. Prior experience executing capital projects. Working knowledge of analytical testing preferred; demonstrated experience with quality engineering methodology desired.
Only on-line resumes will be accepted.
If you require accommodation under the American?s with Disabilities Act to apply for this position,
contact Suzanne Drew (402) 467-8808. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Principle Medical Scientific Expert MD (CV) |
| Education:
? MD with unique knowledge for successful clinical program development and execution, with ? 3 years of clinical research experience required. Preference for 2+ years of industry experience
Or
? MD with specialty with board certification or equivalent required.
Languages:
Fluent English (oral and written)
Experience:
? Advanced medical/scientific writing and communication skills.
? Proven ability to interpret, discuss and represent efficacy and safety data relating to the assigned area (Cardiovascular)
? Proven ability to work both independently or in a cross functional team setting, including a matrix environment.
? Demonstrated ability to establish effective working relationship with key investigators in assigned TA (CV).
? Medical and/or scientific expertise within the Cardiovascular disease area. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Principal Scientist - Salt and Polymorphism Expert |
| Education (minimum/desirable):
Minimum: BS/MS organic/analytical chemistry with 7-10 years of experience in solid state chemistry of APIs.
Desirable: Ph.D. organic/analytical chemistry or equivalent education with strong emphasis on solid state chemistry with 3-5 years of experience in pharmaceutical industry (knowledge of molecular modeling and GMPs would be a plus). Experience with form selection, polymorphism, and physicochemical characterization of APIs. Familiarity with current analytical instrumentation and techniques to characterize API forms using FBRM, XRPD, DSC, TGA, vibrational spectroscopy, UV-Vis, vapor sorption, GC, HPLC, size and solubility measurement, with an emphasis on laboratory automation. Excellent written and verbal communication skills. Good project management, time management, and decision making skills.
Languages: Fluent English (oral and written)
Experience/Professional requirement:
1. Successfully demonstrated several years (minimum of 3 years)of directly related experience as senior scientist or equivalent in pharmaceutical R&D.
2. Documented scientific/technical expertise in form selection, polymorphism, and characterization of APIs.
3. Successfully demonstrated track record of creativity and problem solving in projects.
4. Proven track record in utilization of special tools/equipment, lab automation tools and specialized facilities.
5. Profound literature search skills.
6. Strong presentation skills and scientific/technical writing skills.
7. Proven scientific leadership skills.
8. Ability to work in interdisciplinary teams.
9. Familiarity with the current analytical instrumentation and techniques to characterize crystalline and amorphous materials.
10. Familiarity with GLPs as applied to pharmaceutical industry. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Principal Clinical Scientist |
| Education:
O.D. degree (or equivalent)
Experience:
4 years in product development and/or research.
Skills:
Working knowledge of experimental design, clinical trial im-plementation and management, and data analysis.
Proficient in MS Word, Excel, and PowerPoint.
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Presidential Post Doctoral Fellow |
| Multiple positions exist at all sites of Novartis Institutes for BioMedical Research for individuals with the following minimum requirements: Ph.D. in biological sciences, chemistry, or computer science. Applicants who have commenced postdoctoral training may apply as well, but they should not have been in postdoctoral training for more than 3 years. Candidates must be able to work independently and also participate in team efforts. Excellent oral / written communication and presentation skills and scientific creativity are essential. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| PhD Scientist: Ophthalmology Pharmacology: Target ID/Validation |
| The ideal candidate will have a Ph.D. in Developmental Biology, Cell Biology, Immunology or Ophthalmology with 3-5 years of relevant post doctoral training and demonstrated expertise in molecular mechanisms and pathways. A solid background in ophthalmology research is preferred. Strong organizational, leadership and both oral and written communication skills, along with a track record of scientific accomplishments and a desire to work in a team focused environment are essential. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| PhD Scientist: Antibody Therapeutics |
| Molecular Biology lab head Qualifications:
? Ph.D. in molecular biology or life science
? Minimum 3 years of post-doctoral experience in life-science and/or antibody therapeutic research. Industry experience is a plus.
? Self-driven and creative personality
? Excellent written and oral communication skills
? Extensive experience in molecular biology, cell and biochemical assay development and analysis |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| PhD Scientist- Oncology Biology |
| Qualifications:
? Ph.D. molecular biology or related field
? Minimum 3 years of post-doctoral experience in cancer biology
? Working knowledge of basic cancer signaling pathways
? Independent, self motivated and innovative
? Excellent written and oral communication skills
? Experience in cell and biochemical assay development and analysis
? Excellent interpersonal skills; track record of success working collaboratively |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| PhD Medicinal/Synthetic Organic Chemist |
| * Ph.D. in synthetic organic or medicinal chemistry
* relevant post doc or up to 10 years of industrial experience
* Experience managing BS/MS chemists
* Proven track record of innovative project contributions including peer-reviewed publications
* Ability to work independently and ability to interact with a multidisciplinary team of medicinal chemists, biologists, pharmacologists and external collaborators.
* Experience with modern structure-based drug design and multi-parallel synthesis is a plus.
* Excellent oral / written communication and presentation skills
* Flexibility to work in a dynamic environment |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Pharmacogenetic Analyst |
| Competencies:
? Strong background in genetics and/or molecular biology
? Previous experience performing genetic association studies required
? Strong background in biostatistics and/or statistical genetics
? SAS programming a plus
? Proficiency working with and manipulating large data sets
? Broad scientific knowledge
? Experience in clinical development desirable
? Ability to work well in a team environment
? Excellent presentation and communication skills (essential)
? Strong publication record desirable
Education and professional experience:
PhD in genetics (or related fields) is required with experience performing genetic/genomic association studies. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Pathways Cellular/Molecular Scientist (BS/MS) |
| Minimum requirements MS in Biochemistry, Molecular Biology, Cell Biology, with 5-10 years of laboratory research experience.
? Thoroughly familiar with culturing various mammalian cell lines and primary cells, generating stable cell lines, designing cell-based and biochemical assays, and executing small molecule screens.
? Outstanding molecular biology techniques including DNA cloning, DNA/RNA preparation and characterization (SB, NB, qPCR).
? Exceptional expertise in genetic screening with siRNA/shRNA/cDNA by conventional and viral transduction technologies.
? Proficient in various techniques of protein expression, purification and functional characterization (WB, Co-IP, ELISA, luciferase assay).
? Experience with fluorescent imaging, flow cytometry.
? Excellent communication skills and usage of data analysis software. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Patent Attorney |
| Minimum education: B.A., B.Sc. (or equivalent), chemistry, biochemistry or equivalent with strong understanding of medicinal chemistry in a biotech/pharma environment. M.S., Ph.D. or equivalent in organic or medicinal chemistry preferred.
J.D. or equivalent; Admission to at least one state bar; and Registered to practice before Patent Office.
? Expertise in local patent law; Detailed understanding of global patent systems (including but not limited to US, EP, JP and international systems), patent process, documentation and national and international patent office filing systems.
? Strong scientific background.
? Strong customer-service focus to build and sustain good working partnerships with key stakeholders and project teams.
? Effective analytical, presentation and communication skills.
? Demonstrated ability to work independently as well as collaboratively in a team.
? Well-developed research and critical thinking skills, and sound decision-making abilities, with attention to detail to produce consistently accurate work.
? Strong organization and time management skills with flexibility, creativity, resourcefulness to successfully prioritize and manage multiple, competing priorities simultaneously.
? Strong written and spoken communication in English is required. Proficiency in other languages, such as German, a plus. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Patent Agent II (Pharma Division) |
| ? Bachelor's Degree or higher in Chemistry, Biochemistry or other relevant scientific discipline.
? US Patent Agent Registration to practice
? Minimum 5 years' experience in patent prosecution in a corporate or law firm setting specific to chemical, pharmaceutical or healthcare industry
? Must be able to understand and apply basic patent law principles and procedures
? Excellent written and oral communication skills
? Ability to communicate clearly in a cross-functional and multinational environment and with employees of different levels within the company
? A small amount of travel to meetings and conferences may be required (about 5%). |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Oncology Pharmacologist BS/MS Scientist |
| B.A/B.S. or technical equivalent with expertise in in vivo physiology or pharmacology. Industry experience with oncology models is strongly preferred. Individuals with experience in molecular biology techniques are strongly encouraged to apply.
Candidates will be expected to possess:
? Hands on in vivo skills necessary to validate and implement rodent oncology models including dosing and tumor implantation techniques. Experience with models derived from primary patient samples a plus.
? Demonstrated ability to quickly learn and perform in new areas, implement new techniques and instrumentation.
? Meticulous laboratory approach, careful adherence to protocol and excellent lab notebook documentation
? Strong analytical and computer skills
? Strong oral and written communication skills
? Demonstrated team player. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Oncology Global Drug Development Fellow |
| Qualifications required
Medical Doctorate (MD) degree or equivalent is required.
Advanced knowledge in Oncology, Haematology, Endocrinology required. Completion of 2-4 years of post-MD training in above area required.
Fluent oral and written English. Any other language a plus.
Knowledge, Skills, and Experience desired
Involvement in patient care and demonstrated medical/scientific expertise in oncology and/or haematology
Exposure to or demonstrated interest and knowledge in pharmaceutical company research environment
Strong interpersonal, communication, and problem solving skills.
Demonstration of general understanding of drug development process including key processes involved in protocol development, clinical trial conduct, statistical analysis of trials, and regulatory environment,
Demonstration of ability to work within a team environment and across other functions
Mobility/Citizenship
Must be able to relocate to Basel, Switzerland or New Jersey, USA for a period of one year
Current residency/citizenship of an EU country is highly preferred.
Must be able to attain the appropriate work authorization for the US in a timely fashion.
For US and Switzerland, Novartis will apply on the candidate?s behalf. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Oncology Director/Sr. Director Global Medical Affairs |
| MD required. Board certified hematologist/oncologist preferred. Advanced knowledge of oncology required. Must have >5 years of demonstrated leadership and accomplishment in clinical trials and/or medical affairs (planning, executing, reporting clinical trials, leading medical affairs activities) in academia/pharmaceutical industry. Strong leadership, management, interpersonal, communication, negotiation, and problem-solving skills. Ability to think strategically. Organizational awareness (inter-relationship of departments, business priorities), and experience working on cross functional teams desired. Excellent written and oral communication skills, including presentation skills. Fluent oral and written English. Ability to interact effectively with external customers and internal stakeholders. Ability to travel, US and International. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Oncology Director Medical Affairs |
| MD with board-eligibility or certification in oncology or hematology preferred. Advanced knowledge of oncology required. Must have >2 years of demonstrated leadership and accomplishment in clinical trials and/or medical affairs (planning, executing, reporting clinical trials, leading medical affairs activities) in pharmaceutical industry. Team player attitude is necessary. Prior staff management experience is a plus. Ability to communicate and partner with global marketing and medical colleagues as well as study investigators. Ability to travel both domestically and internationally is required. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Onco Sr Dir Clinical Res Phys |
| The successful candidate will be required to have Board Certification in Oncology and Hematology with a minimum of 2+ year of industry experience managing clinical research or 5+ years of relevant medical/clinical experience.
? Experience in previous management and accountability for budget execution is desirable.
? Previous experience in collaborative interactions on clinical studies with investigators globally is very important
? Previous experience managing CRO interactions related to clinical study operations is highly desirable.
? Candidates should have demonstrated the capability for strategic planning along with operational skill and experience related to clinical research involving both single and multiple centers. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Onco Sr Dir Clinical Res Phys |
| The successful candidate will be required to have Board Certification in Oncology and Hematology with a minimum of 2+ year of industry experience managing clinical research or 5+ years of relevant medical/clinical experience.
? Experience in previous management and accountability for budget execution is desirable.
? Previous experience in collaborative interactions on clinical studies with investigators globally is very important
? Previous experience managing CRO interactions related to clinical study operations is highly desirable.
? Candidates should have demonstrated the capability for strategic planning along with operational skill and experience related to clinical research involving both single and multiple centers. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| NIBR Search Network, Application Manager |
| Qualifications:
? Advanced degree in Computer Science
? At least 3-5 years experience in Application Management
? Sound Knowledge of Search and Web Technologies
? At least 1 year of experience with the Fast ESP platform
? Strong communications and interpersonal skills
? Ability to work independently and as part of a team
? Work with different NITAS groups that work in close coordination with TMS e.g. Omega, Data and Middleware Management Services in RCP and the NITAS Help Desk in the US.
Reporting
The candidate will be part of the Text Mining Services Group, one of the IS (information services) groups in NITAS and will report to the Head of Text Mining Services located in Basel. The role is based in Cambridge, Massachusetts. The candidate will be a member of the NIBR Search team and work under the direction of the NIBR Search project leader. |
| Novartis Oncology |
na |
IL |
9/4/2010
|
| National Account Scientific Directpr |
| MD, PharmD, or PhD with 4 years Post-Doctoral experience required or relevant experience. Oncology experience required. Managed care & outcomes research experience preferred. Field based medical experience in the pharmaceutical industry preferred. Thorough knowledge of clinical medicine, the managed markets, pharmacoeconomics, disease management, and medical research. Excellent interpersonal communication and presentation skills, (including ability to network), strong personal integrity, teamwork abilities and a customer focus are necessary. Must possess a thorough understanding of the FDA, OIG, HIPAA, and GCP/ICH guidelines relevant to the pharmaceutical industry. Must be able to organize, prioritize, and work effectively in a constantly changing environment. Strong working knowledge of the organization of Microsoft Office Suite (Word, PowerPoint, Excel, Access). Ability to interface effectively with a variety of technical platforms for the collection, review, and dissemination of medical information. Demonstrated record of scientific/medical publication. Demonstrated knowledge of GCP practices and standards. Demonstrated technical expertise in oncology. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Molecular/Cell Biology Research Associate (BS/MS) |
| B.S/M.S. degree with over 3 years of lab experience and strong background in cell biology, biochemistry and molecular biology. Previous experience in the study of innate immunity is highly desirable. Experience with large dataset analysis is a plus. The candidate is expected to possess strong problem solving and analytical skills, and be capable of independent, creative thinking. Excellent communication and organization skills are required. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Molecular Phenotyping Scientist |
| Applicants should hold a BS degree in biology (or related fields) with 2 plus years experience as research histologist in the bio-pharmaceutical industry or biomedical research. A very good understanding and practical experience of special histology techniques and immunohistochemistry applied to pre-clinical research is essential. Excellent knowledge of molecular biology concepts applicable to research histology in order to select appropriate reagents and assay design is highly desirable. An excellent capacity and adaptability to learn new techniques under the direction of more senior laboratory peers is required. Previous experience in digital slide scanning and image analysis applied to tissue sections is a plus. Excellent organizational skills in daily laboratory activities are essential. Good interpersonal skills and capacity to conduct laboratory activities in a dynamic cross-functional research environment is essential. Excellent computer skills with daily experience with Microsoft Office environment are also required. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Molecular Pathways Investigator (Ph.D) |
| Ph. D. degree with 1- 3 years of postdoctoral training and with strong background in cell biology, biochemistry and molecular biology. Previous experience with identification and progression of biological targets is a plus. The candidate is expected to possess strong problem solving and analytical skills, and be capable of independent, creative thinking. Excellent communication and organization skills are required. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Molecular Pathway Biology Research Scientist (BS/MS) |
| BS or MS scientist with 3-5 years of laboratory research experience.
? Thorough familiarity with culturing various mammalian cell lines and primary cells, generating stable cell lines, designing cell-based and biochemical assays, and executing small molecule screens.
? Outstanding molecular biology techniques including DNA cloning, DNA/RNA/protein isolation and characterization.
? Expertise in genetic screening with siRNA/shRNA/cDNA by conventional and viral transduction technologies.
? Excellent communication skills and usage of data analysis and repository software.
? Eagerness and flexibility to learn new techniques, a positive team orientation, and genuine scientific curiosity are a must. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Molecular Pathologist, Investigative Toxicology |
| Education
? MD or DVM, board-certified pathologist or equivalent
and
? PhD or equivalent scientific records in life sciences
Experience
? Extensive operational knowledge of gene expression analysis from tissues
? Proficient data interpretation techniques applicable to toxicology
? Knowledge in toxicology and/or toxicologic pathology
? Significant scientific experience working in molecular pathology or molecular toxicology
? Hands-on experience in immunohistochemistry/in situ hybridization,image analysis, and gene expression profiling
? Excellent data summarization: used to presenting clearly and simply complex data or phenomena
? Excellent oral and written English communication skills. Able to present and defend data and influence the decision process regarding study design
? Experience organizing labs
? A results-driven self-starter and decision taker; open, confident and persuasive, succeeding through influence
? A creative and innovative approach with a sharp and objective intellect, experienced in balancing big picture thinking with detailed analysis
? Strong cooperative team player, ability to be flexible and adapt to a changing environment
? A commercial outlook; used to helping a business achieve its objectives
? Well developed interpersonal skills
? Good planning, prioritisation, problem solving and organisational skills
? Resilient, energetic and enthusiastic; responding constructively to challenging new ideas and inputs |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Molecular and Cellular Biology Research Scientist (BS/MS) |
| ? B.S/M.S. in Biochemistry, Cell Biology or Molecular Biology
? Minimum 5 years experience in biochemistry, mammalian cell biology working with various cell lines and/or cell signaling mechanisms
? Previous experience with stable cell line production, design and analysis of cell-based assays, transfection and viral transduction technologies and RNAi techniques is required.
? Proficiency in the use of molecular biology and protein biochemistry technologies, e.g. DNA cloning, Real-time PCR, protein-protein interaction, and enzymatic assays is preferred.
? Familiar with different technologies to monitor cellular events (proliferation assays, high content imaging, technologies to monitor the state of signaling molecules in cellular extracts).
? Must be highly motivated, team-oriented, and have excellent interpersonal and communication skills. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Mgr/Associate Director, Audit and Monitoring (Ethics and Compliance) |
| B.A. degree; experience in audit; CPA and/or CFE certification preferred.
KNOWLEDGE AND SKILL REQUIREMENTS:
1. Knowledge of audit techniques including risk analysis identification skills.
2. 5-10 years experience with at least 3 years in the pharmaceutical industry conducting complex, sensitive and essential (ad-hoc and required) audit and monitoring activity related to pharmaceutical fraud and abuse and regulatory non-compliance in order to identify individual conduct issues as well as overall program enhancement opportunities (e.g., policy, training, etc).
3. Strong interpersonal, communication, and presentation skills. Requires political savvy and the ability to take difficult or unpopular positions when necessary to protect the company.
4. Visibility requires maintaining an even temper and treating all persons with respect to project a positive image at all times despite stress or other circumstances.
5. Solid knowledge of Federal health care regulations, FDA and OIG laws/guidelines in relation to compliance program administration within the pharmaceutical industry.
6. Candidate must have the proven ability to evaluate trends, organize and conduct multiple, simultaneous audit and monitoring initiatives, deal tactfully with others, prepare accurate and sound reports, and coordinate with many cross-functional stakeholders to achieve identified outcomes.
7. Ability to travel 40%. |
| Novartis Oncology |
na |
CA |
9/4/2010
|
| Mfg Process Engineer - Vacaville, Calif |
| BS in Chemical, Biochemical, or Mechanical Engineering, preference in Chemical/Biochemical Engineering.
Written and spoken English
Up to 5 years in a commercial manufacturing environment |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Medical Scientific Expert |
| Education: MD required with unique knowledge for successful clinical program development and execution required.
Languages: Fluent English (oral and written)
Experience:
? Advanced medical/scientific writing and communication skills.
? Proven ability to interpret, discuss and represent efficacy and safety data relating to the assigned area.
? Proven ability to work both independently or in a cross functional team setting, including a matrix environment.
? Clinical research experience preferred.
? Medical and/or scientific expertise within a disease area preferred. Preference for previous experience with Heart Failure or Thrombosis focused work. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Medical Science Liaison (MSL) Hematology - New Jersey |
| Position will be filled at level commensurate with experience. Advanced scientific degree required (MD, PhD, or PharmD highly preferred). Minimum of 5 years Oncology experience with a strong current working knowledge of Oncology required. Teaching experience preferred. Previous pharmaceutical industry experience preferred. Thought leader development experience is a plus. Knowledge of treatment guidelines, clinical research processes, FDA regulations and OIG guidelines is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important external customers, including medical thought leaders, academic institutions, large group practices, medical directors and pharmacy directors is required. Must be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Must be a strong team player who can effectively interface cross-functionally with Novartis clinical and commercial personnel. Working knowledge of Microsoft Office Suite (Word, PowerPoint, Excel) and associated hardware is required. The position is associated with approximately 60% travel. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Medical Director/Senior Medical Director, Psychiatry, US Medical |
| A MD or DO degree with 3-5 years of pharmaceutical industry experience is required; Board Certification/Eligibility in Psychiatry and clinical/research background in Psychiatry would be a plus.
? Experience in managing clinical trial conduct for psychiatric disorders is essential.
? Firm working knowledge of GCP, scientific and clinical methodology, protocol design, project management and regulatory requirements for clinical studies designated for review by regulatory authorities.
? Medical Affairs and U.S. marketing experience, to include a well documented history in medical development of Psychiatric therapeutics and of bridging proactive relationships among product development, clinical development and marketing teams.
? A well-established network within the medical research community that will attract high-caliber professionals into the Novartis organization.
? Proven ability to build productive relationships and teams internally and externally, and the ability to develop high potential subordinates into leadership roles.
? Reputation as an open, available and transparent communicator.
? Strong leadership and organizational skills; demonstrated personnel management capabilities.
? Excellent oral and written communication skills.
? Experience leading large projects/organizations.
? Ability to travel (U.S. and European; 20-25% annually. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Medical Dir/Sr Medl Dir,Primary Care, US Medical(Arthritis/Immunology) |
| ? A MD or DO degree with 3-5 years of pharmaceutical industry experience is required; Board Certification/Eligibility in Internal Medicine and clinical/research background in rheumatology would be a plus.
? Experience in managing clinical trial conduct for rheumatologic disorders is essential.
Firm working knowledge of GCP, scientific and clinical methodology, protocol design, project management and regulatory requirements for clinical studies designated for review by regulatory authorities.
? Medical Affairs and U.S. marketing experience, to include a well documented history in medical development of rheumatology therapeutics and of bridging proactive relationships among product development, clinical development and marketing teams.
? A well-established network within the medical research community that will attract high-caliber professionals into the Novartis organization.
? Proven ability to build productive relationships and teams internally and externally, and the ability to develop high potential subordinates into leadership roles.
? Reputation as an open, available and transparent communicator.
? Strong leadership and organizational skills; demonstrated personnel management capabilities.
? Excellent oral and written communication skills.
? Experience leading large projects/organizations.
?Ability to travel (U.S. and European; 20-25% annually). |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Medical Dir/Sr Medical Director US Medical NSO (Multiple Sclerosis) |
| A MD degree with 3-5 years? pharmaceutical industry experience is required; Board Certification/Eligibility in Neurology and clinical/ research background in Multiple Sclerosis will be a plus.
? Experience in managing clinical trial conduct for neurological disorders and Multiple Sclerosis is essential.
? Firm working knowledge of GCP, scientific and clinical methodology, protocol design, project management and regulatory requirements for clinical studies designated for review by regulatory authorities.
? Medical Affairs and U.S. marketing experience, to include a well documented history in medical development of Multiple Sclerosis/ Neuroscience therapeutics and of bridging proactive relationships among product development, clinical development and marketing teams.
? A well-established network within the medical research community that will attract high-caliber professionals into the Novartis organization.
? Proven ability to build productive relationships and teams internally and externally, and the ability to develop high potential subordinates into leadership roles.
? Reputation as an open, available and transparent communicator.
? Strong leadership and organizational skills; demonstrated personnel management capabilities.
? Excellent oral and written communication skills.
? Experience leading large projects/organizations.
? Ability to travel (U.S. and European; 20-25% annually, up to 40% seasonally). |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Medical Dir/Sr Med Dir RTI, US Medical, (Transplantation/Immunology) |
| Position will be filled at level commensurate with experience:
? A MD or DO degree with 3-5 years of pharmaceutical industry experience is required; Board Certification/Eligibility in Internal Medicine and clinical/research background in transplantation would be a plus.
? Experience in managing clinical trial conduct for transplantation is essential.
Firm working knowledge of GCP, scientific and clinical methodology, protocol design, project management and regulatory requirements for clinical studies designated for review by regulatory authorities.
? Medical Affairs and U.S. marketing experience, to include a well documented history in medical development of transplantation (preferred) or immunology therapeutics and of bridging proactive relationships among product development, clinical development and marketing teams.
? A well-established network within the medical research community that will attract high-caliber professionals into the Novartis organization.
? Proven ability to build productive relationships and teams internally and externally, and the ability to develop high potential subordinates into leadership roles.
? Reputation as an open, available and transparent communicator.
? Strong leadership and organizational skills; demonstrated personnel management capabilities.
? Excellent oral and written communication skills.
? Experience leading large projects/organizations.
?Ability to travel (U.S. and European; 20-25% annually). |
| Novartis Oncology |
na |
NE |
9/4/2010
|
| Mechanical Technician |
| ? Associates degree in either Electromechanical Technology or Machine Tool Technology and 3 years related experience. Preferred: Electromechanical Technology.
? Must pass a hands-on mechanical skills test.
? Demonstrated skill in the use of machine tools and hand tools.
? Welding skills to include stainless steel, aluminum, and mild steel.
? Knowledge of electrical systems, safety compliance, and personal computers (Excel, Word, Internet).
? Skill in interpreting and applying specifications, blueprints, engineering drawings, and work instructions in order to perform installation, repair, and modification work.
? Preferred knowledge of pharmaceutical manufacturing process equipment and systems including automated material handling of solids and liquids, lean manufacturing practices, Good Manufacturing Practices (GMP?s), and Standard Operating Procedures (SOP?s) including validation issues and change control processes.
? Good oral and written communication skills.
If you require accommodation under the American's with Disabilities Act to apply for this position, please contact Suzanne Drew at (402) 467-8808. |
| Novartis Oncology |
na |
CA |
9/4/2010
|
| Manufacturing Mechanic - Vacaville, California |
| Minimum 5 years experience as a Master Maintenance Mechanic or equivalent.
?Must have 3 years experience troubleshooting industrial mechanical systems and electrical systems.
?Demonstrated thorough knowledge of general maintenance procedures (Trade School, Apprenticeship or directly applicable experience).
Additional requirements:
?Must have pertinent experience in 3 of the following disciplines: Plumbing, pipe fitting, welding, electrical, refrigeration, HVAC, machinist, steam fitter, or boiler mechanic.
?Requires handling of chemicals such as acids, alkalis, solvents and powered media.
?Able to work in noisy environments that may exceed 80 decibels.
?Must be able to wear negative pressure based respirator.
?May be required to lift up to 50 pounds multiple times in the work shift (i.e., 1-5 times in a hour)
?Requires bending and reaching throughout the work shift in support of wide range of activities such as valve adjustment, fastening of hoses and/or connections and conducting cleaning activities.
?May require climbing up and down flights of stairs during the work shift (i.e., 1-4 times in a hour) as well as ascending a fixed or portable ladder to heights up to twenty feet.
?Requires walking/standing for extended periods (up to 6 hours) throughout the work shift.
?Must be able to enter confined spaces such as tanks and pits.
?May need to adapt to changing work shifts, both swing and/or graveyard on very short notice. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Manager/Associate Director, Strategic Sourcing |
| Degree (minimum), MBA (desirable)
English (minimum), other languages (desirable)
High level of experience in Strategic Sourcing and Category Management; high level of experience in managing cross functional teams in complex organisational matrix
5 years experience in strategic sourcing
Desirable if experienced in clinical/scientific spend sourcing |
| Novartis Oncology |
na |
NC |
9/4/2010
|
| Manager, Validation |
| ?BS degree in a physical science such as engineering, chemistry, biology required with 7 ? 10 years experience.
?Solid dosage and generics experience preferred.
?Prior experience leading multi-disciplined teams. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Manager, Area Sales - NYC |
| To be successful as the Area Sales Manager, the right candidate will need to have a 4 year college degree plus 7 to 10 years of professional sales experience in the healthcare field, advanced degrees preferred. The preference would be to have had experience selling biologic injectables and/or growth hormone / endocrine products to physicians and health plans |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Manager, Advanced Computing Operations |
| -VMWare and Clusters
-Citrix / Xenapp Application Publishing
-Core IT Infrastrucutre Service delivery:
o Patching
o Perfomance Monitoring,
o Capacity Planning
-Excellent written and oral communication skills
-Organized approach to solution delivery
Demonstrated Success
-Candidates will be required to demonstrate proven capabilities in all aspects of this demanding opportunity.
-Present an operations plan along with reporting and the business life- cycle.
-Prepared to diagram a request and provisioning process to demonstrate experience with successful enterprise level service delivery |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Manager Clinical Data Mgt |
| Education
BA/BS degree in life science, computer science, pharmacy, nursing or related scientific fields
Experience/Professional
requirement:
1. 6+ or more years of experience in drug development with at least 5 years in Data Management
activities from a pharmaceutical or biotechnology firm.
2. 2 years of established line management or project team leadership experience.
3. Strong technical and problem solving skills.
4. Excellent understanding of clinical trials methodology,
GCP and medical terminology.
5. Ability to work independently, under pressure, demonstrating initiative and flexibility through effective and innovative leadership ability.
6. Attention to detail and quality focused.
7. Strong organizational, planning, resource and project management skills.
8. Strong interpersonal and communication skills,and ability to operate effectively in an international environment.
9. Strong negotiation and diplomacy skills.
10. Excellent understanding of physiology, pharmacology and clinical study objectives and the drug development process.
11. Ability to mentor & coach within DM and cross functionally, and to train in internal and external processes.
12. Strong people management skills with positive leadership, innovative, and collaborative behaviors. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Manager Business Planning |
| ? BS/BA in Finance with MBA and/or CPA preferred
? 3-5 years relevant Finance experience with demonstrated achievement in roles of increasing responsibility
? Strong Excel and Powerpoint skills required with working knowledge of SAP R3, Business Warehouse and TM1 desirable
? Results focus with the ability to work independently to meet targets and deadlines
? Excellent analytical capabilities required with consistent attention to details
? Strong interpersonal skills with the ability to productively challenge the status quo and to lead and influence across functions
? Excellent verbal and written communications abilities with capacity to clearly present and discuss financial issues at all levels of management and with non-finance business partners |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Manager Engineering Systems |
| BS/MS in Engineering (Biomedical/ Bioengineering, Mechanical, Electronic, Chemical, Systems) with minimum of 7 years experience in Life sciences or medical device development.
In-vitro molecular diagnostics experience essential. Familiar with regulatory and compliance requirements for diagnostic tests. Experience in engineering design, optics, hardware, system architecture, application support, and disposables. Minimum 2 years in role as systems engineer or system analyst. Experience working on multi-disciplinary projects. Strong knowledge of assay chemistry for diagnostic tests/molecular biology. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Knowledge Engineering/Text Mining Expert |
| Qualifications:
? Higher education, such as an advanced degree in a business discipline related to life sciences (e.g. biology, bio-informatics, genetics). In-depth knowledge of automated information extraction and/or text mining techniques, computational linguistic analysis and their application to scientific textual data, computational lexicons.
? Concrete experience of problems associated with biomedical and pharmaceutical terminology and data
? Web-oriented technologies and programming languages (Java, Perl, XML, HTML, JavaScript, CGI, etc.)
? 5 years of Knowledge Engineering or Text Mining working experience.
? Recognized Knowledge Engineering/Text Mining Expert.
? Understand the business environment of the business areas to be supported within and outside of NIBR. The business environment includes knowledge of business strategy, objectives, capabilities, processes, data, information, roles fulfilled during drug development, and organizational structures, understanding of influences external to a business organization, such as competitors, regulatory requirements, best in class practices and economic factors.
Reporting
The candidate will be part of the Text Mining Services Group, one of the IS (information services) groups in NITAS and will report to the Head of Text Mining Services located in Basel. The role is based in Cambridge, Massachusetts. The candidate will be member of the team of Knowledge Engineers. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| IT Business Analyst, Business Support Operations |
| BSc in scientific or IT related discipline; advanced degree preferred
-6+ years experience in IT, proven business analysis skills
-Excellent people, analytical, written/verbal/presentation communication skills
-Experience with agile software development methodology
-Experience in life sciences industry desirable
-Knowledge of drug discovery & development process desirable
-Experience and knowledge in document, information lifecycle, knowledge and records management systems preferred |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| IS Business Process Analysis Site Lead, (Account Management) |
| -BSc in scientific or IT-related discipline; advanced degree preferred
-Proven senior stakeholder relationship management skills in a complex, geographically distributed organization
-Experience and knowledge in document, information lifecycle, knowledge and records management systems
-Strong operational (managing projects/services) and vendor & supplier management skills
-Evidence of business systems strategy development & execution
-Excellent people, leadership, analytical, written/verbal/presentation communication skills
-Experience with agile software development methodology
-Minimum 3 years management experience in an IT role of similar size & complexity; 7-10 years total experience
-Experience in life sciences industry desirable |
| Novartis Oncology |
na |
CO |
9/4/2010
|
| IPQA Associate II/III - 3rd Shift |
| Educational/Professional Requirements:
? Bachelor degree in a science or engineering field
? Minimum 2 years QA/QC experience
? cGMP experience required
? Trackwise/SAP experience a plus
? Pharmaceutical manufacturing experience a plus
Skills & Competencies:
? Maintains positive attitude and team focus
? Must be able to multi-task and change priorities with minimal interruption.
? Requires skills in change management, negotiation, conflict resolution and collaboration with others
? Maintains high level of professionalism and acts as a calming influence in all situations
? Vigilant to ensure compliance to cGMPs, site policies and procedures and regulatory requirements |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Investigator II - Sr Investigator I |
| Ph.D., Pharm. D or MS degree in pharmacokinetics, biopharmaceutics or related sciences. The knowledge of tissue distribution, radiochemistry, metabolism and pharmacokinetics is highly desirable. The candidate should be able to provide technical assistance on individual projects, spanning across multiple therapeutic areas. Hands-on experience in PK and PK/PD analysis and modeling is a must. Prior work experience with PK/PD analysis and a demonstrated ability to work with modeling tools and databases (e.g. WinNonlin, GastroPlus, Watson, Spotfire, etc). The candidate must be able to work independently and excellent oral and written communication skills are required. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Investigator ? M.D., PhD, Cardiovascular and Metabolic Diseases (CVM) |
| The candidate is required to have a M.D. or MD/PhD with at least 8 years of relevant postdoctoral training in a clinical research organization or teaching hospital or related pharmaceutical clinical experience. Clinical training should be in one of the following areas: cardiology, endocrinology, gastroenterology, metabolic syndrome, or type II diabetes The candidate should have strong leadership skills, a proven track-record of scientific achievement including quality publications, demonstrated ability to work in an interdisciplinary team setting, and experience supervising and training technical level staff. Broad scientific knowledge, strong work ethic, excellent oral and written communication is essential. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| In Vivo Pharmacology Lab Leader: Cardiovascular & Metabolic Disease |
| PhD with a minimum of three years of research in physiology, pharmacology or closely related discipline.
?General knowledge of state-of-the-art technologies, platforms and approaches which enable practical yet innovative ways to support drug discovery programs.
?Thorough understanding of diabetes, metabolism or cardiovascular in vivo models. Clear understanding of in vivo drug metabolism, pharmacokinetics, and pharmacodynamics.
?Strong command of academic, commercial research efforts, scientific literature, and knowledge of key opinion leaders in the area. Candidates with expertise in Cardiovascular and Metabolic disorders are preferred.
The successful candidate for In Vivo Pharmacology Laboratory Leader will be a decisive and results-oriented individual who is flexible, team-oriented, creative and able to excel in a multi-project, fast-track environment. He or she will be a strategic thinker who interacts and collaborates with project teams, peers and management in identifying and achieving discovery goals from both scientific and strategic perspectives. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| In vivo and Molecular Biology Research Associate (BS/MS) |
| The candidate should have a BS/BA or Master?s degree in biology or related field, with extensive animal handling experience, broad molecular biology expertise, and data management skills. Experience with rodent models of human cancers, including xenografts and/or endogenous models, is particularly desired, as well as experience with in vivo xenogen imaging. Previous demonstration of independence, in experimental design and problem-solving, is required. The candidate must communicate and work well in a team environment. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Imaging Physician Project Leader |
| ? Ph.D. with minimum 10 years of relevant experi-ence in Imaging or Allied Health Sciences in de-velopment & implementation of imaging strate-gies for pre-clinical, translational or clinical pro-grams in oncology clinical trial.
?
OR
? MD/PhD with relevant Board Certification in Diag-nostic Radiology or Nuclear Medicine with a mini-mum of 4 years of relevant experience in devel-opment & implementation of imaging strategies for pre-clinical, translational or clinical programs in oncology clinical trial.
? Knowledge in pathway based molecular imaging essential.
? .Knowledge of clinical and translational imaging validation against survival and biological end-points is essential
? Strong understanding of biostatistics and bioin-formatics
? An understanding of assay technologies and the requirements for validation is desirable
? Ability to work in a team environment
? Experience in working in a global matrix envi-ronment
? Ability to work on multiple projects and under strict deadlines
? Excellent oral/written/presentation communica-tion skills both internally and externally.
? Ability to write Clinical Study Protocols, report and publications.
? Familiarity with the content and development of standardized imaging protocols (RECIST, Cheson) |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| IIRP Manager (Sr Clin Rsrch Scientist)-US Medical, Transplant Med Unit |
| The requirements include a minimum of a BSN or RN, BA or BS in a scientific discipline, and at least 5 years of clinical research experience in a pharmaceutical environment. A minimum of five - seven years relevant experience in a clinical research/drug development environment is required for a Sr CRS position. A background in pharmaceutical industry research in the Transplant Therapeutic Area is preferred, but is not required. Effective oral and written communication skills are a must. The demonstrated ability to independently write Clinical Trial Protocols is preferred. The ability to work both independently and collaboratively on Project teams and to recognize safety and efficacy data trends is essential. Strong budget management is required. Knowledge and experience of clinical trial design, analysis, and reporting is also necessary. The Sr CRS should be familiar with all aspects of the drug development process and have knowledge of the medical, scientific and clinical research techniques of the assigned area. Working knowledge of GCP and local regulatory requirements is desired. The ability to travel up to 10% is also required. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| IIRP Manager (Sr Clin Rsrch Scientist)-US Medical, MS Medical Unit |
| The requirements include a minimum of a BSN or RN, BA or BS in a scientific discipline, and at least 5 years of clinical research experience in a pharmaceutical environment. A minimum of five - seven years relevant experience in a clinical research/drug development environment is required for a Sr CRS position. A background in pharmaceutical industry research in the MS therapeutic area is preferred, but is not required. Effective oral and written communication skills are a must. The demonstrated ability to independently write Clinical Trial Protocols is preferred. The ability to work both independently and collaboratively on Project teams and to recognize safety and efficacy data trends is essential. Strong budget management is required. Knowledge and experience of clinical trial design, analysis, and reporting is also necessary. The Sr CRS should be familiar with all aspects of the drug development process and have knowledge of the medical, scientific and clinical research techniques of the assigned area. Working knowledge of GCP and local regulatory requirements is desired. The ability to travel up to 10% is also required. |
| Novartis Oncology |
na |
CA |
9/4/2010
|
| Head of Manufacturing Technology (Process Sciences)- Vacaville, CA |
| -PhD in Microbiology, Biochemistry, Biochemical/Chemical Engineering
-English required; German or French desirable
-Minimum of 5 years in a commercial manufacturing environment |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Group Head -IMS |
| Medical Degree required. Specialty board certification desir-able. Ancillary degree in toxicology, pharmacology, or genetics useful. ? 3 years clinical experience postdoctoral
? At least 7 years in drug development in a major pharma-ceutical company (of which 5 years in a global position), including 5 years in safety at an operational or medical po-sition
? Experience in early clinical development/translational medicine and in due diligences
? Experience in preparing of clinical safety assessments and regulatory reports/submissions involving safety informa-tion.
? Track-record in leading cross-functional teams and people management
? Experience in drug development, clinical trial methodology, regulatory requirements, scientific methodology, statistics and writing of publications
? Desirable: Management experience |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Global Program Medical Director |
| ? MD required. Advanced knowledge in medical/scientific area required.
Languages:
Fluent oral and written English
Experience/Professional requirement:
? ? 10 years of involvement in drug development spanning clinical activities in Phases II/IV or comparable experience in industry.
? ? 5 years of demonstrated leadership and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing), or section of clinical programs in a global/matrix environment (including remote) in pharmaceutical industry.
? ? 5 years people management experience required, this may include management in a matrix environment. Global people management experience desirable.
? Strong management, interpersonal, communication, negotiation and problem solving skills.
? Considerable organizational awareness (e.g., inter-relationship of departments, business priorities), including significant experience working cross-functionally and in global teams.
? Medical/scientific and operational expertise appropriate to the program.
? Demonstrated technical knowledge and innovation in clinical development study designs that provide relevant evidence to decision-makers.
? Prior history with post-marketing/brand optimization studies to obtain evidence of brand value and support commercialization activities preferred. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Global Program Diagnostics Director |
| Education:
Doctoral in life sciences or chemistry, or MBA with equivalent experience in life sciences.
Languages:
Fluent English (written and oral), on other language.
Experience/Professional Requirements:
1. 12+ years industry experience
2. 5+ years multi/cross functional leadership experience within an Oncology business unit.
3. International drug or diagnostic development project functional leadership
4. Have an advanced understanding of the diagnostic development process and programs.
5. Provide thought-leading insights to the competitive environment and internal partner interfaces
6. Sound knowledge of international customs and business practice
7. Hands on experience with a major submission and regulatory review process
8. Proven people leadership capabilities
9. Model natural leadership characteristics
10. Expert leadership skills demonstrated in GPT, in staff management role or in other organisational assignments. Expert skills to facilitate/optimise contribution of team members as individuals and members of cohesive team.
11. Strong interpersonal and communication skills for bridging scientific and business participants, for negotiating timelines and for effective international collaboration.
12. Outstanding verbal and written communications.
13. Diagnostic experience is an advantage
14. Results driven |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Global Medical Monitor |
| Education Requirements:
Doctor of Optometry or MD.
Experience Requirements:
5 to 8 years clinical or industry experience
Experience working with medical devices in a regulated environment is highly desirable.
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Global Lead, Informatics Systems Adoption |
| Competencies/Experiences Needed...
* experience delivering modern approaches to educating groups and individuals in software, to include but not limited to virtual and web based learning
* experience working in an environment where change is the norm
* ability to focus on execution while maintaining and advancing clear strategies, goals and accountabilities
* must have built teams and created relationships with a wide variety of customers both internal and external
* have a network of vendors that you can bring to table and utilize within our organization
* experienced at creating the future vision for software training & adoption
* able to set priorities, make decisions and lead the team to meet those priorities |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Global Head/Director -Biostatistics |
| At least PhD in Statistics (or equivalent degree/knowledge/expertise).Usually 8 years of relevant experience in the
Pharmaceutical Industry.
2. Experience as Project Statistician for International
Clinical Teams.
3. Very strong skills in leading people, operations,
and innovation.
4. Expert knowledge in clinical trial methodology,
and in statistics and its application in clinical trials.
5. Excellent knowledge of drug development and
commercialization process and relevant guidelines
and processes.
6. Project Management skills.
7. Excellent communication skills.
8. Background medical knowledge, preferably in
relation to the specific therapeutic area. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Global Head, Scientific and Clinical Education |
| Education:
? MD and/or PhD degree in the life sciences, public health or related fields
Languages:
? Strong command of written and spoken English is a must.
Experience:
? Several years of work experience in a biomedical research environment (corporate, academic, government or non-profit) Direct pharmaceutical experience will be a key plus.
? Strong interest in and track-record of developing and delivering scientific/clinical training and education programs to a range of audiences
? International work experience and/or experience working in a multicultural environment a must.
? Strong leadership skills, including influencing and coaching skills; highly experienced in change management; strong project management skills and ability to work in a highly matrixed environment are essential
? Proven ability to conduct needs assessments, develop and implement targeted programs/solutions, and to define and measure success of complex interventions
? Excellent negotiation, communications (oral and written) and presentation skills are required;
? Expected travel: Up to 35% domestic/international. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Global Head Scientific Support Translational Sciences |
| PhD in Biostatics or Life Sciences
Proven track record at global leadership level for at least one of Biostatistics, Data Management, Programming for a Therapeutic Area and demonstrated global leadership role for at least one of the remaining disciplines.
Strong leadership of multi-disciplinary drug development projects and change leadership intiatives. Expert skills in leveraging and maximising the contribution of diverse team members as both single contributors and as a cohesive, efficient team
Languages:Excellent English required (oral & written). Good skills in site (local) language desired (oral).
Experience/Professional requirement: Significant relevant experience in the Pharmacetical industry.
Minimum 10+ in drug development. Five ? seven years leading global teams and global departments (or local sites). |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Global Head of Innovation, Quality, Productivity (Lean Six Sigma) |
| Bachelor?s degree (desired in engineering)
Master?s degree preferred(Engineering or MBA),
Demonstrated formal Statistics and Lean training, Certified Lean Six Sigma Master Black Belt, Change Management and Train the Trainer training desirable
Minimum Experience:
10 years+ Manufacturing experience with a minimum 5 years in managerial capacity.
7+ Years experience as a practicing Black / Master Black Belt.
3+ years experience as Director of Lean Six Sigma.
Experience with multi-site leadership and support.
Demonstrate delivering measureable results in leadership of large multi-site projects.
Experience in developing and delivering Lean Six Sigma training to Black and Green Belts.
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Expert Statistician Translational Sciences |
| University degree in Statistics or Mathematics (Ph.D. or MSc. Level)
At least five years of relevant experience in the field of clinical trials
Strong statistical skills and knowledge of clinical trials methodology
fluent in English, written and spoken
Experience gained in all main tasks of a Senior Statistician, and experience as project statistician for international clinical teams or comparable experience in similar ED role.
Good leadership skills.
Very good project management skills.
Very good communication and presentation skills
Good knowledge of the drug development process and relevant HA guidelines.
Basic coaching and mentoring skills.
Good team player.
Strong knowledge and expertise in statistics and its applications in clinical trials.
Experience with implementation of novel methods and/or innovative strategies |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Expert Statistician Shanghai China |
| Minimum Requirements
? At least Master?s Degree in statistics or a closely related field.
? At least 7 years of experience in drug development (4 years for Ph.D.).
? Solid knowledge and experience in drug development and Health Authority guidelines.
? Prior experience in dealing with health authorities desired.
? Good command of English, written and spoken.
? Ability to manage projects and supervise other team members
? Work or college experience in another country or demonstrated ability working together in a multicultural organization desired.
? Advanced knowledge of statistical software, in particular SAS. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Expert Modeler |
| Ph.D. Degree in a modeling-related field with 6 years of relevant experience, or equivalent degree/expertise.
1. Experience in applying M&S to drug R&D in at least two of the following applied areas: biology, pharmacology and/or statistics
2. In-depth knowledge in several of the following modeling areas, and knowledge in others: learning algorithms, molecular pathways, biology, tissue effects, physiology and pathophysiology, PK/PD, statistics, pharmacology, toxicology, pharmaceutical R&D process.
3. Solid knowledge of the drug R&D process, including clinical development; background medical knowledge and substantial PK/PD knowledge; modeling and HA guidelines, as relevant to M&S.
4. In-depth knowledge of and experience with relevant software packages
5. Good data exploration skills. Ability to understand heterogeneous data.
6. Ability to communicate effectively with people from diverse scientific backgrounds in a multi-disciplinary organization; ability to interact effectively with both management and teams to constructively influence decision-making
7. Exceptional written and verbal communication skills including the ability to interact effectively with a multidisciplinary team
8. Good business ethics
9. Innovative attitude; creative approach to model implementation; welcomes problems as challenges; able to approach problems from multiple angles
10. Well-developed organizational skills; able to manage several projects simultaneously. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Expert Clinical Manager (CVM) |
| Education:
? Advanced degree or equivalent education/degree in life science/healthcare required accompanied with ? 2 years experience in clinical research.
or
? Bachelor degree or equivalent education/degree in life science/healthcare required if accompanied with ? 4 years experience in clinical research.
Languages:
Fluent English (oral and written)
Experience:
? Involvement in cross-functional, multicultural and international clinical trial teams; demonstrated capabilities in leading specific trial related activities like planning, executing, reporting and publishing activities.
? Excellent communication, organization and tracking skills. Strong operational skills and demonstrated ability to meet timelines.
? Proven networking skills and ability to train colleagues.
? Proven ability to work both independently or in a team setting, including a matrix environment
? Knowledge of Good Clinical Practice; thorough knowledge of clinical trial design; understanding of the overall drug development process.
? Knowledge of principles for trial budgeting.
? Basic knowledge of TA preferable. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Expert Clinical Manager |
| Phase I Oncology clinical trial experience a requirement. On an exception basis highly-qualified candidates with strong oncology experience with Phase 2/3 clinical trial experience might also be considered. Candidates should have 3-5 years of experience in clinical environment (at least 2+ pharma. industry). University degree in Biological Sciences/Nursing/Pharmacy is a minimum. Candidates must demonstrate:
* strong oral and written communications skills and experience in medical scientific writing protocols and Clinical Trial Reports independently
* experience and ability to recognize safety and efficacy data trends independently
* knowledge of clinical trial design, statistics and pharmacokinetics
* experienced with all aspects of the drug development process
* knowledge of medical, scientific and clinical research techniques of the assigned areas
* knowledge of GCP and local regulatory requirements |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Expert Clinical Manager |
| Phase I Oncology clinical trial experience a requirement. On an exception basis highly-qualified candidates with strong oncology experience with Phase 2/3 clinical trial experience might also be considered. Candidates should have 3-5 years of experience in clinical environment (at least 2+ pharma. industry). University degree in Biological Sciences/Nursing/Pharmacy is a minimum. Candidates must demonstrate:
* strong oral and written communications skills and experience in medical scientific writing protocols and Clinical Trial Reports independently
* experience and ability to recognize safety and efficacy data trends independently
* knowledge of clinical trial design, statistics and pharmacokinetics
* experienced with all aspects of the drug development process
* knowledge of medical, scientific and clinical research techniques of the assigned areas
* knowledge of GCP and local regulatory requirements |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Expert Auditor |
| BA/BS or equivalent
Advance degree desirable
English fluency at operational and functional level (as first or second language; second language a plus)
5 plus years PV/clinical/industry/health authority experience with GCP/PV auditing experience;
40 % travel;
Ability to independently manage and objectively evaluate complex compliance issues with minimal supervision;
Ability to address a variety of tasks within the same timeframe while maintaining oversight; ability to maintain a high degree of independence with respect to decision making and problem solving;
Extensive experience with Health Authority inspections and interaction;
Excellent quality and compliance leadership and facilitation skills;
Excellent verbal and written communication, organizational and interpersonal skills;
Excellent computer skills, including Excel, Word, etc;
Extensive knowledge of applicable PV, GCP and GxP regulations, guidelines, policies and procedures;
Good knowledge of computer validation and Part 11 requirements;
Ability to lead teams and operate successfully in various team capacities;
Ability to operate successfully in various cultural environments;
Ability to deputize for Group Head as needed;
Auditor certification desired. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Exec Director Oncology Scientific Affairs |
| ? M.D. Degree is preferred; individuals holding a Ph.D or PharmD degree who have a broad clinical science background in Oncology will be considered.
? Prior strategic leadership experience of geographically dispersed teams in the pharmaceutical or biotechnology industry.
? Proactive people leadership, as demonstrated by a history of setting clear goals for direct reports and coaching for maximum performance.
? Advanced proficiency in stakeholder management, including interpersonal skills and customer service orientation.
? Applied understanding of and ability to integrate health economics and outcomes research into new customer programs and initiatives
? Ability to shape and implement customer-centric medical strategies in Oncology Business Unit.
? Ability to lead in a highly matrixed environment and influence internal partners to achieve desired business outcomes.
? Strong cross-functional, collaboration and negotiating skills.
? Advanced knowledge of the US market and the stakeholders influencing medical decisions.
? Thorough understanding of the FDA, OIG, HIPAA and other ethical guidelines relevant to the pharmaceutical industry, and to ensure compliance with these external as well as internal guidelines and standard operating procedures.
? Ability to interface effectively with a variety of technical platforms for the collection, review, and communication of medical information
? Demonstrated a record of Scientific/Medical publications |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Ex Dir Medical Expert Oncology |
| ? MD, preferably MD/PhD, with board certification in Medical Oncology or Hematology/ Oncology required. Additional advanced degrees in Life Science disciplines a plus.
? Minimum 5 years of clinical trial experience that includes trial design and conduct required.
? Experience in biomarker development, and in regulatory submission/review process preferred.
? Prior work experience within a global business environment is a plus.
? Strong interpersonal and verbal/written communication skills required, ability to bridge scientific with business communication and strong negotiation skills a plus.
? A results oriented personality with strong desire to advance to higher levels of responsibility within the organization is a plus. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Epigenetics Research Scientist (BS/MS) |
| Applicants must have B.S. or M.S. degree in Molecular Biology, Cell Biology, Biochemistry, or a related discipline and have a minimum of three years of work experience.
? Proficiency with mammalian cell culture, including stable cell line production, FACS, transfection and viral transduction technologies, and genetic knockdown techniques using RNAi
? Proficiency in molecular biology, including cloning strategies, site-directed mutagenesis, construction of reporter systems, design and use of various expression vectors, measurement of protein and mRNA expression, and chromatin immunoprecipitation
? Experience with cellular assays measuring cell proliferation, cell cycle, migration/invasion, senescence and /or apoptosis via immunofluorescence imaging and other methods
? Must be detail oriented and able to handle multiple tasks efficiently
? Proven track record in handling, recording, and quantitatively analyzing experimental data |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| eCRF Dev Sr Specialist |
| BA / BS degree in Computer Science, Mathematics, Life Science, Medical Informatics or equivalent degree. Ideally 3-5 years of experience in clinical
programming, set-up of clinical databases and CRF Design, gained in pharmaceutical industry or CRO as well as the following: Strong knowledge of database support: Oracle OC/RDC, PL/SQL, or equivalent clinical database
management system. Strong knowledge of reporting support: SAS, PL/SQL or other equivalent ad -hoc query and reporting tools.
Excellent understanding of clinical database management systems and/or relational databases as applied to clinical trials. Strong ability to analyze the impact of changes to clinical
standards, with minimal supervision. Strong ability to multi- task. Strong ability to be able to switch between different tools for database design, reporting and management.
Strong understanding of ICH and Health Authority guidelines and regulations as they pertain to clinical database management, clinical data reporting and
computer systems. Expert attention to all of the following: detail, quality, timelines and customer focus. Strong ability to work to deadlines independently. Strong communications skills required in order to be able to work with a wide variety of global customers
both face-to -face and via phone or e-mail.
SAS experience strongly preferred. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| DSM Trial Manager |
| 1. At least 4 years of relevant experience in Pharmaceutical
Development, Clinical Development, Clinical Supply
Operations, Project Management or Related Field.
2. Excellent organization and planning skills.
3. Good and leadership skills.
4. Excellent communication, negotiation and interpersonal
skills.
5. Ability to strategically plan, organize and manage multiple
projects simultaneously.
6. Recognized knowledge of clinical supplies.
7. Successfully demonstrates track record of creativity
and problem solving in projects.
8. Demonstrates working knowledge of clinical supply
systems and specialized tools.
9. Advanced knowledge of development activities and
processes.
10. Advanced project management skills.
11. Advanced presentation skills. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Director, Synthesis and Formulation |
| Education Requirements:
Ph.D. in Chemistry, Polymer Chemistry, Chemical Engineering, Polymer Science & Engineering, Materials Science, or related field
Experience Requirements:
15+ years exp, preferably in regulated industry
Requires strong management and communication skills, as well as team and cross-functional project leadership capability. Must be able to multi-task and effectively work in a diverse environment.
Position has a global focus, therefore previous experience working with colleagues outside the US is a preferred qualification. Position may require some international travel and domestic travel.
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
NC |
9/4/2010
|
| Director, Engineering - Wilson, NC |
| Bachelor?s Degree in an Engineering discipline (Chemical, Electrical or Mechanical Engineering
preferred); At least 10 - 12 years experience at management and a senior level Engineering
position preferred (leading site Engineering, leading large Engineering projects,
etc.)Comprehensive technical knowledge of pharmaceutical equipment and plant design;
Comprehensive equipment and plant control systems understanding (distributed control
systems, local and high speed equipment control, building management systems); Experience
with pharmaceutical industry standards and requirements (Minimum US GMP); Thorough
knowledge of the validation process and Sarbanes Oxley Act (SOX) regulations. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Director, Corp Integrity Agreement Management (Ethics & Compliance) |
| ? Ten to fifteen years experience, preferably in a pharmaceutical / healthcare compliance-focused role. The ideal candidate would possess CIA management experience; however, commensurate project management experience will be considered. Includes managing project timelines, acquiring and managing resources, and ensuring quality deliverables.
? Minimum requirement of BS or BA. An advance degree is a plus.
? Supervisory experience is required
? Ability to work cross-functionally in a collaborative environment, jointly enhancing and developing business processes, policies and procedures. Must be able to implement and drive change management initiatives.
? Strong communication skills; verbal, written and presentation. Must be able to communicate across all levels of the organization.
? Budget oversight and management
? Compliance subject matter expertise, including familiarity with industry codes, laws and regulations
? Must possess strong business acumen, along with being technologically savvy
? Strong policy and process expertise and the ability to apply specific category knowledge to compliance strategy and objectives (e.g. sales and marketing practices, research, clinical and developmental operations)
? Ability to travel(approximately 10%). |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Director, Clinical and Product Training |
| - Bachelors Degree. Advanced degree preferred.
- Strong business background, with a minimum of 7 plus years of work experience;
- Minimum 2 years experience in Sales Management experience and
minimum of 2 years marketing experience.
- Brand strategy, tactics understanding combined with strong clinical & therapeutic knowledge
- Strong overall sales acumen and business experience.
- Excellent problem solving, communication, listening, and facilitation, planning, team building and communication skills.
- Ability to lead teams. Leadership, management skills and executive presence.
- Team player capable of working in large cross functional teams (such as build relationships with sales and marketing organization at all levels)
- Ability to drive and influencing change.
- Some overnight travel required
- Knowledge of pharmaceutical segment and prior training experience preferred |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Director Regulatory Affairs |
| Advanced degree in life-sciences, engineering or public health.
1. Greater than 7 years work related profession experience in diagnostic regulatory affairs
2. 3+ years experience in drug/diagnostic regulatory affairs.
3. 5+ years multi/cross functional leadership experience in clinical development, preferably in molecular diagnostics
4. Knowledge of drug development and regulation affairs requirements
5. Familiar with regulatory issues and challenges associated with Drug/Diagnostic co-development and companion diagnostics.
6. Have a track record in successful FDA and ROW premarket submissions and registrations
7. Solid understanding of molecular technologies and the impact on outcomes and diagnostic results
8. Leadership capabilities working across varied cultures, expertise and backgrounds
9. Excellent negotiation skills with regulatory staff on various levels of hierarchy
10. Outstanding interpersonal and communication skills for bridging scientific and business participants, for negotiating timelines and for effective international collaboration. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Director of Professional Development & Field Implementation (U.S.) |
| Experience Requirements:
8 - 10 years clinical practice or industry experience.
Proven track record of managing department or group of individuals.
Basic understanding of Marketing concepts.
Experience as an officer or Board Member of a Professional Association / Organization (preferred).
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Director of Medical Affairs and Consultation- North America |
| OD or MD degree required
Residency Trained (optional)
Experience Requirements:
8 - 10 years clinical practice or industry experience.
Regulatory experience required.
Basic understanding of Marketing concepts.
Clinical study experience(preferred).
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Director of Clinical Insights |
| Education Requirements:
Ph.D./O.D. and generally 8+ years experience in related field
OR
MS/MA and generally 11+ years experience in related field
Preferred Experience Level:
Working knowledge of regulations and guidelines for the conduct of clinical trials.
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
GA |
9/4/2010
|
| Director Clinical Quality Assurance |
| Education Requirements:
Degree in Biomedical Science or related scientific discipline. Higher degree desirable. O.D. desired.
Experience Requirements:
Minimum 15 years of Pharmaceutical/ Medical Device experience with at least two years in clinical safety or in a regulatory/compliance related area of responsibility.
Thorough understanding of the device development process.
Demonstrated effectiveness in matrixed, cross-functional environments.
Highly developed leadership skills, demonstrated effectiveness in managing associates across geographical boundaries.
Ability to reconcile worldwide safety compliance and GCP requirements with business goals.
Highly developed communication skills with good written and oral command of English.
Highly effective negotiation and presentation skills.
Demonstrated sensitivity and understanding of cultural differences and diversity issues.
As a CIBA VISION associate, you are expected to know, understand, and comply with all applicable safety and health standards and rules.
CIBA VISION is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Dir. Clinical Research Medical Oncologist and or Hematologist |
| The successful candidate will possess MD Board Certified in Oncology/Hematology is strongly preferred. An MD with training in Oncology with a minimum of 3 years of clinical trial experience esp. in later stages of development will also be considered. Experience leading the design, content, analysis and reporting of oncology clinical studies is strongly desirable.
Significant successful interactions with oncology key opinion leaders/investigators.
Candidates should have demonstrated the capability for strategic planning along with operational skill and experience related to clinical research involving both single and multiple centers.
Ability to work across multiple functions is essential. Effective oral and written communication skills and strong leadership are strongly desirable competencies for this role. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Dir IT Program Manager |
| Masters degree in computer science or related discipline, at least ten, typically twelve or more years of solid, diverse work experience in IT, or an equivalent combination of education and work experience. 8+ years of pharmaceutical industry especially within R&D, and 6-8 years of experience in drug regulatory publishing and document management. Experienced program manager of large scale multi-year program with estimated team size 75+ associates (IT, business, externals), and program budget approximately 50-75M USD.
? Strong problem solving capabilities: ability to define approach to any type of problem in a pro-active way
? Leadership skills:
o ability to lead a ?virtual? team in a matrix organization and to interact at management and operational level,
o credibility in both business and IT
o address significant business challenges
? Financial skills: business case follow up and financial reporting
? Experienced working in matrix, multi-disciplinary organization driving significant change and business process transformation and working with many stakeholders on all levels (Pharma Global, Development, Corporate); business consultancy engagements a plus
? Previous background/experience in program management ? at least 10 years ? with track record of results (on time, on budget, on customer satisfaction)
? Experienced with management of project teams globally situated
? Strong knowledge of document and submission management business processes and document standards for regulatory submissions particular to the FDA or other Health Authority new drug product applications.
? Excellent Presentation & communication skills: executive board level
? Strong organization and negotiation skills
? Must have a broad industry knowledge, preferably in Health Care/Pharmaceuticals
? Must have excellent understanding of IT and Computer System Validation in a regulated industry
?Previous experience working on Documentum projects is a plus. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Developmental and Molecular Pathways Biocurator (Ph.D) |
| The successful candidate will have a Ph.D. in biology or a related field.
Along with a proven track record of curating data in a medically relevant field, the candidate should possess:
?Excellent interpersonal and communication skills
?Broad knowledge of research and data analysis methods
?Experience with developing and using ontologies and vocabularies
?Experience with ?omic data analysis
?Experience in molecular pathway/network tools
?Experience with Perl (or other scripting languages), SQL, and relational databases an advantage
?Knowledge of Spotfire, R/Bioconductor, Pipeline Pilot, or Matlab an advantage
?3+ years of industry experience preferred |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Developmental and Molecular Pathways Assay Development Scientist |
| The candidate should have a B.S. or M.S. degree or equivalent in biochemistry, cell biology, engineering or similar with 3+ years of industrial or academic research. Must be highly collaborative, self-motivated, results focused, team-oriented, and have excellent communication and computer skills. |
| Novartis Oncology |
na |
CA |
9/4/2010
|
| Development Scientist |
| * Bachelor's degree in science or engineering discipline or similar
* Fluent in speaking / writing in English
? 1-3 years experience in pharmaceutical/biotech with production in a GMP facility
? Demonstrated experience and competencies in fermentation and protein recovery or protein recovery and purification
? Ability to manage smaller projects
? Ability to handle multiple projects simultaneously under tight deadlines
? Working knowledge of Good Laboratory/Manufacturing Practices, regulations, regulatory compliance requirements and current industry standards
? Strong verbal and written communication skills |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Data Manager, Clinical Pharmacogenetics |
| Competencies:
? Detail-oriented
? Strong quantitative skills
? Strong organizational skills
? Strong multitasking skills
? Strong communication and collaborative skills
? Knowledge of SAS scripting
? Good writing skills
? Familiarity with basic methods of statistical analysis a plus
Education and professional experience:
Masters Degree with at least 2 years experience or Bachelor?s Degree with at least 4 years experience managing or working intensively with health care or biotech data. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| CTH/ Sr. CTH |
| ? ? 6 years technical, operational and managerial experience in planning, executing, reporting and publishing clinical studies in a pharmaceutical company or contract research organisation.
? Experience in multiple clinical indications and/or TAs is preferable.
? Previous experience leading in parallel several trials; leading multidisciplinary trial teams in a complex matrix environment (including remote).
? Demonstrated ability to establish effective working relationships with key investigators.
? Thorough knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes, and global clinical development process.
? Advanced knowledge of the assigned TA is preferred, with the demonstrated capability to interpret, discuss and represent trial or program level data.
? Previous experience in interactions with Health Authorities is preferable including submission experience |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| CTH (nonMD) |
| Phase I Oncology clinical trial experience a requirement. On an exception basis highly-qualified candidates with strong oncology experience with Phase 2/3 clinical trial experience might also be considered. Candidates should have 3-5 years of experience in clinical environment (at least 2+ pharma. industry). University degree in Biological Sciences/Nursing/Pharmacy is a minimum. Candidates must demonstrate:
* strong oral and written communications skills and experience in medical scientific writing protocols and Clinical Trial Reports independently
* experience and ability to recognize safety and efficacy data trends independently
* knowledge of clinical trial design, statistics and pharmacokinetics
* experienced with all aspects of the drug development process
* knowledge of medical, scientific and clinical research techniques of the assigned areas
* knowledge of GCP and local regulatory requirements |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| CTH (NonMD) |
| Phase I Oncology clinical trial experience a requirement. On an exception basis highly-qualified candidates with strong oncology experience with Phase 2/3 clinical trial experience might also be considered. Candidates should have 3-5 years of experience in clinical environment (at least 2+ pharma. industry). University degree in Biological Sciences/Nursing/Pharmacy is a minimum. Candidates must demonstrate:
* strong oral and written communications skills and experience in medical scientific writing protocols and Clinical Trial Reports independently
* experience and ability to recognize safety and efficacy data trends independently
* knowledge of clinical trial design, statistics and pharmacokinetics
* experienced with all aspects of the drug development process
* knowledge of medical, scientific and clinical research techniques of the assigned areas
* knowledge of GCP and local regulatory requirements |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Contracts Specialist Coordinator II |
| Degree in business administration, finance, science or related field or equivalent on the job experience maybe considered. High degree of organizational, analytical, and team management skills. Computer literacy with document and spreadsheet applications. Ability to work on complex, multi-faceted projects. Excellent negotiation skills and vast knowledge of clinical trial agreements. Minimum seven years experience in pharmaceutical services with five years contract management and/or study start-up activities including contract negotiations and management. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Computer Aided Drug Design (Ph.D) |
| We are looking for a range of computational skill sets and experience levels. We invite interest from both experienced PhD/postdoctoral level computational drug discovery scientists (<10 years industry/biotech) as well as newly qualified PhD/postdoctoral computational scientists. In building a dynamic and interactive CADD team we anticipate bringing complementary skills together. We are therefore interested in a range of backgrounds; structure and ligand based design, homology modeling, ADME/tox modeling, QSAR and chemoinformatics are some of the preferred areas of expertise. You will use the appropriate blend of chemical and biological knowledge with state-of-the-art computational software technology to understand molecular data through visualization, prediction and analysis of trends in the 'drug-hunting' process and, in collaboration with a wide variety of multi-disciplinary scientists, devise creative solutions to drug discovery problems and new paths toward medicines.
Minimum requirements: Natural team-working ethic together with excellent communication and influencing skills. An ability to devise innovative drug-discovery solutions and follow through in their implementation. Strong programming skills are a plus. Advanced knowledge of one or more of the following: structure and ligand based drug design, molecular dynamics, docking methods, pharmacophore hypothesis generation and elucidation, binding free-energy relationships, quantum mechanics, conformational analysis, QSAR, SAR analysis of HTS data, chemical libraries design. A strong grounding in synthetic organic chemistry, physical chemistry and structural biology. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Computational Biologist (Ph.D) |
| The successful candidate will have a Ph.D. in biology, computational biology, or a related field, and 1 to 3+ years of related experience.
Along with a proven track record of formulating, testing and communicating biological hypotheses, the candidate should possess:
?Excellent interpersonal and communication skills
?A solid understanding of basic statistics and quantitative data analysis
?Experience with ?omic data analysis
?Experience in molecular pathway/network analysis
?Experience with comparative genomics
?Experience with High Throughput Sequencing (NGS)
?Expertise working in Unix/Linux and Windows environments
?Experience with Perl (or other scripting languages), SQL, and relational databases an advantage
?Knowledge of Spotfire, R/Bioconductor, Pipeline Pilot, or Matlab an advantage |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Clinical Research Manager |
| Education: Bachelor?s degree in life science/healthcare is strongly recommended.
Languages: Fluent English ? Oral and written
Experience/Professional requirement:
? 4 years technical, operational and managerial experience in planning, executing, reporting and publishing clinical studies in a pharmaceutical company or contract research organisation.
Proven ability to work independently, to lead a multidisciplinary trial team in a complex matrix environment (including remote).
Experience in developing effective relationships with key team members including investigators.
Thorough knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes, and global clinical development process.
Oncology and/or Hematology background is preferable. Health science background is strongly recommend. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Clinical Program Leader (MD) |
| MD Required. Need 3-5 pharma/biotech industry experience in drug development - clinical trials. Must have Phase I Oncology proof-of-concept clinical trial designs expertise. Knowledge of PK/PD and basic statistics. Proven ability to analyze and interpret efficacy and safety data relating to assigned area Medical/scientific writing skills. Knowledge of GCP and world wide regulatory requirements relating to assigned area. Effective written and oral communication skills. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Clinical Education Director |
| MD (Dr. Med) with a working knowledge of early drug development, as well as clinical trials experience is required. Candidates with M.D./Ph.D. as well as biotech/ pharmaceutical experience would be favorably considered. In addition, we are looking for candidates who have some or all of the following: research experience in life sciences, clinical sciences, or pharmacology; supervision of postdoctoral fellows; experience in initiating scientific/medical education or training programs. Domestic and international travel will be required. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Cell Pharmacology Lab Leader: Cardiovascular and Metabolic Diseases |
| ?PhD with a minimum of three years of research in cell biology and pharmacology or closely related discipline.
?General knowledge of state-of-the-art technologies, platforms and approaches which enable practical yet innovative ways to support drug discovery programs.
?Thorough understanding of cell-based assay development, assay automation for mid-high throughput cellular assays, ex-vivo cell culture systems and cellular mechanism of action studies to ensure the success of target-driven drug discovery.
?Strong command of academic, commercial research efforts, scientific literature, and knowledge of key opinion leaders in the area. Candidates with expertise in Cardiovascular and Metabolic disorders are preferred.
The successful candidate for Cell Pharmacology Lab Leader will be a decisive and results-oriented individual who is flexible, team-oriented, creative and able to excel in a multi-project, fast-track environment. He or she will be a strategic thinker who interacts and collaborates with project teams, peers and management in identifying and achieving discovery goals from both scientific and strategic perspectives. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| BSL |
| ? 3 years clinical experience postdoctoral
? At least 5 years of experience in drug development in a major pharmaceutical company or CRO, or Health Au-thority, including at least 3 years of experience in clinical safety (of which at least 2 years in a global posi-tion).
? Experience in preparing clinical safety assessments, risk/benefit evaluations and regulatory reports
? Experience in leading cross-functional, multi-cultural teams
? Experience with safety issue management
? Experience in preparing RMPs, PSURs, Submission dos-siers (SCS). |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| BS/MS Scientist: Molecular Microbiology |
| The successful candidate will have a BS or MS degree in molecular biology, biochemistry, or microbiology and at least one year of work relevant work experience. He/she will be a detail-oriented team-player who is able to multitask and effectively organize and analyze data.
Desired skills: must be adept in basic molecular biology techniques such as cloning, restriction digest, plasmid preparation, DNA and protein gel electrophoresis, and PCR. Must have excellent sterile technique and proficiency with either mammalian or microbial cell culture. Experience with enzymology or cell-based assays is a plus. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| BS/MS Scientist: Cell Pharmacology |
| Qualified candidates should possess a BS/MS in biology, biochemistry or related field with at least 3 years of post-graduate experience. Previous experience in an industry setting is a plus. An excellent knowledge of and experience in mammalian cell culture is required. Previous experience in cell based assay development and automation is also preferred. Excellent communication and interpersonal skills and the ability to work effectively in a team environment are essential. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| BS/MS Scientist Cardiovascular & Metabolic Disease: Biologics |
| BS or MS degree in biology, biochemistry, or chemistry with 3 years of experience in molecular biology, prokaryotic and eukaryotic cell culture, protein purification and assay development, preferably in the pharmaceutical or biopharmaceutical industry; experience in cardiovascular and metabolic disease is desirable; broad scientific foundation, strong work ethic, excellent oral and written communication, and ability to function in an interdisciplinary team setting are essential. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| BS/MS Associate: Ocular Imaging |
| The ideal candidate will have a B.S. or M.S. in Biophysics, Biomedical Engineering, Physiology, Vision Science, Pharmacology, or a related field with 2-4 years of relevant experience. Strong organizational skills, exceptional data management, flexibility, and a desire to learn new techniques to contribute in a team environment are essential. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Biostatistician, Gene Expression |
| The successful candidate will have a Ph.D. degree in Biostatistics or Statistics with more than 5 years experience in statistical analysis, including at least 4 years experience in the analysis of gene expression biomarker data preferably in a pharmaceutical setting. A strong background in parametric and nonparametric statistical methods, multivariate statistics, classification and resampling, as well as experience in analysis of biomarker and assay data is required. Experience in predictive modeling, classification and discriminant analysis is also desirable. The candidate should possess strong communication skills with the ability to communicate effectively with statisticians and non-statisticians alike. Experience with R/Bioconductor, and other relevant software packages is a must. Familiarity with a Linux/Unix environment will be a plus. Strong scientific writing skills, collaborative skills and multitasking skills are all key attributes required for this position. |
| Novartis Oncology |
na |
CA |
9/4/2010
|
| Biopharmaceutical Graduate Program - Vacaville, Calif |
| ?Recent MS or Ph.D. program graduate in the life sciences.
?Proven success and demonstrated leadership ability within a previous academic
and/or industrial setting.
?Familiar with the biotech industry, its science and its engineering.
?Must have an awareness of multidimensional/ multivariable differentiation concept and presentation.
?Must be available for worldwide assignment.
?Must have strong interpersonal and communication skills.
?Must be able to multitask effectivel between multiple projects.
?Must be fluent in English and knowledge of German or French would be a plus. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Bioinformatics, Business Analyst (Translational Sciences/ETL Tools) |
| ?Bachelor's degree in computer science and/or advanced degree in biology
?At least 3-5 years experience in application development in a drug discovery, scientific or biotech environment
?Basic understanding of regulatory requirements/compliance policies (e.g. GLP)
?Strong communications and interpersonal skills
?Solid understanding of ETL tools
?Proven capabilities interacting with scientists and being customer service oriented
?Ability to work independently and/or as part of a team
?Knowledge in biology, biological research processes, and applications
?Good understanding and practical experience in fundamentals of software engineering
?Solid understanding of relational databases and familiarity with Oracle and/or SQL server |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Bioinformatics Scientist - Oncology Research |
| MS or higher in bioinformatics or a related field, with a minimum of 5 years research experience, are required. Strong scientific programming skills are required, with experience in Perl, the R statistical language and/or Matlab strongly preferred. The ideal candidate will demonstrate a strong understanding of the application of data mining techniques to genomic data sets (including expression, copy number, and next generation sequencing). Strong communication skills and a proven track record of interacting with scientific teams are essential. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Bioinformatician/Translational Sciences (CONTRACT) |
| The successful candidate will have a Ph.D. in bioinformatics, engineering, physics, statistics, applied mathematics, or a related field with a strong computational background. The successful candidate will have experience (2+ years) analyzing genome-scale data sets and a working knowledge of molecular biology. Fluency in at least one statistical package (R/Bioconductor preferred) and one programming or scripting language (e.g. Perl, Ruby, Java, Python) is a must. Experience in Linux environments and clusters is also required. Familiarity with software packages such as Bowtie, Partek, Bfast, GATK, Velvet, Galaxy, IGV, Partek, and Matlad is also required. The successful candidate will be a team player with good communications skills, capable of discussing complex computational concepts with scientists from a variety of backgrounds. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Bioinformatician |
| Education (minimum/desirable):
BA/BS or MA/MS in computer science or information technology
Languages: Fluent English
Oral and written
Experience/Professional requirement:
1.3-5 years prototyping computational solutions in an industry or academic setting
2.1-2 years experience with developing web tools in an industry or academic setting
3.1-2 years experience with current database software tools
(eg, Oracle, MySql, SciBase)
4.1-2 years experience with bioinformatics tools and resources
5.Experience with relevant scripting and development tools
(eg, Pipeline Pilot, Perl/Python, Java, Javascript, Unix/Linux)
6.Excellent multitasking and prioritization skills
7.A ?self starter? who will take ownership of projects
8.Demonstrated user/customer focus |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| Biobanking Project Manager |
| PhD, or PharmD
Languages: Fluent English (verbal and written)
Experience of min. 2+ years pharmaceutical or biotech industry experience. Previous experience in a multi-disciplinary environment.
Knowledge of translational/clinical science.
Understanding of the drug development process.
Laboratory experience in handling biological samples and biomarker analysis.
Team player with demonstrated ability to build collaborative relationships.
Strong interpersonal and communcation skills for managing timelines, budget and resources and for effective internal collaboration.
Excellent verbal and written communication skills.
Expertise in Microsoft Office, Microsoft Sharepoint, and Lotus Notes are necessary. |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| BioAnalytical Mass Spectrometry Scientist |
| A BS/MS with 2+ years of relevant experience in mass spectrometry. A strong background in separations is required. Knowledge of assay development and experience in the use of liquid handling systems is desired, as is the desire to be trained in new methodologies and technologies. Excellent communication skills and the ability to multitask in a fast-paced environment are essential. Previous experience in the analysis of proteins and/or in the preparation of cell lysates is a plus, but not necessary |
| Novartis Oncology |
na |
CA |
9/4/2010
|
| Automation Engineer |
| Minimum of 5 years experience in a similar position is required for the Automation Engineer and 10 years experience in a similar position is required for Senior Automation Engineer. Experience in Pharmaceutical or Biotechnology is a plus. The ideal candidate will have a proven track record in engineering leadership as well as the ability to develop and implement standard engineering practices, as well as provide detailed documentation upon project completion. This person will be the project technical lead and may be responsible for some project management activities. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Associate Scientist-Formulator |
| Qualifications
Working knowledge in the use of the solid dosage form manufacturing processes such as wet granulation, roller compaction, melt extrusion and compression. Experience in formulation including scientific knowledge of formulations, physico-chemical and biopharmaceutical principals underlying pharmaceutical dosage forms.
Able to interpret data to draw appropriate conclusions and recommended additional experiments under moderate supervision; good oral and scientific writing skills; good time management skills; effective team player and good multitasker; able to quickly adapt to changing work requirements, assignments and environments.
Languages: Fluent English (oral and written)
Education: An MS candidate with 0-2 years or a BS candidate with 0-4 years experience in pharmaceutical development. Degree in a scientific or relevant discipline (e.g., Chemistry, Pharmacy, Chemical Engineering). |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Associate II, Regulatory Affairs |
| Language Skills
Good oral and written communication skills
Education and Experience
Candidate must possess a Bachelor?s degree and 3+ years experience in the pharmaceutical industry. IT and eCTD experience is highly preferred. Experience within a Regulatory Affairs Department is also a plus. |
| Novartis Oncology |
na |
WA |
9/4/2010
|
| Asc Dir Regional Training (West Region) - Psychiatry Franchise |
| ? Bachelor?s degree
? Thorough knowledge of pharmaceutical industry, antipsychotic category, schizophrenia market, and medical service delivery.
? Minimum 2-3 years of successful pharmaceutical sales representative experience
? Mimimum 2 years of first-line sales management experience leading a specialty sales team
? Experience in account based selling
? Excellent planning, organization, and execution; teamwork, information management; judgment and decision making; people development skills, and strong learning orientation.
? High proficiency in communication and presentation skills.
Preferred:
? 1-2 years successful institutional/specialty sales experience, preferably in psychiatry institutions and Community Mental Health Centers (CMHCs) or Behavioral Health Organizations
? Sales or marketing experience in psychiatry, preferably schizophrenia
? Certification in education and/or instructional design, Masters degree, MBA or equivalent
? High proficiency in adult learning theory
? Sales Training experiences |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| Asc Dir Product Management |
| Education: Bachelor's Degree. MBA desired but not required.
Related Work Experience: At least 2-3 years of Global Marketing experience |
| Novartis Oncology |
na |
MA |
9/4/2010
|
| ADME/DMPK Investigator (Ph.D) |
| A Ph.D. with 5+ year working experience in ADME, DMPK, or related fields. Good understanding of underlying principles of in silico, in vitro and in vivo ADME especially in drug absorption and transporters are essential. Skills and hands-on experience are required in developing and utilizing in silico ADME/PBPK models (e.g. Simcyp, MetSite, GastroPlus, etc.) and chemoinformatic or statistic tools (e.g. PCA/PLS, QSAR, etc.) to address key ADMET issues for drug discovery research. Successful experience in managing a lab, supervising associates and/or representing ADME/DMPK in drug discovery project teams is highly desirable. He/she should be familiar with important in vitro ADME assays (e.g. PAMPA, Caco-2, transporter phenotyping, etc.), bioanalysis, lab automation and compound/data management. Excellent communications (in both oral and written formats) and favorable teamwork skills are a must. |
| Novartis Oncology |
na |
NJ |
9/4/2010
|
| AD Project Manager, Oncology Clinical Operations |
| A bachelor's degree in Science, Nursing, or Pharmacy. A minimum of five years experience in clinical research and knowledge of the drug development process are required. The candidate must have a thorough understanding of clinical trial conduct and regulation. Strong communication, interpersonal and negotiation skills are essential. Strong computer skills including facility with the Microsoft Office Suite and the ability to extract and analyze data from the clinical trial databases, IMPACT are required. Previous project management experience is preferred. Oncology experience is desired. |
| AstraZeneca Pharmaceuticals |
Waltham |
MA |
9/4/2010
|
| Principal Scientist - Cell/Lead Biologist |
| Minimum Requirements
*PhD and 5+ years experience in cancer cell biology with a minimum of 3 years in the pharmaceutical industry or equivalent
Competencies/Behaviors
*Strong understanding of cell assay development and small molecule drug screening
*Broad understanding of cancer disease biology
*Demonstrated previous authorship of patents and/or peer reviewed publications
*Ability to work in a team-oriented environment
*Strong interpersonal and communication skills
*Effective leadership and management skills
*Delivery focused |
| AstraZeneca Pharmaceuticals |
Waltham |
MA |
9/4/2010
|
| Development Microbiologist (Principal Scientist I) |
| *PhD in microbiology, infection pharmacology, or a related discipline and experience of publishing relevant research in the academic literature.
-5 or more years experience in the microbiology of the clinical development of antibacterial agents.
*Familiarity with the work of CLSI and EUCAST.
*Working knowledge of internet search tools such as Pubmed, Highwire, Google scholar, Science direct, Scifinder etc.
*Experience of creating good scientific proposals and presenting them authoritatively at project meetings.
Skills and Competencies
*Can address the needs of multiple customers: development microbiology directors and colleagues, project team and discovery medicine colleagues, doctors, regulators and patients.
*Holds self and others accountable.
*Self-development orientation: can listen to and respond to feedback and provide constructive feedback to others.
*Ability to work under pressure and to deadlines.
*Good collaborator: respects and integrates different views.
*Ability to analyze data and make consequent recommendations for action.
*Results orientation.
Preferred Background
*PhD in microbiology and a publication track record.
*Seven or more years' experience in the microbiology of the clinical development of antibacterial agents.
*Experience of preparing microbiology plans to support antibacterial drug development projects, including planning non-clinical microbiology in accordance with the project strategy and regulatory guidance.
*Experience of conducting the microbiology associated with clinical trials.
*Experience at presenting microbiology work to project teams to monitor progress against agreed strategies.
*Knowledge of key members of CLSI and EUCAST, and microbiology outsource provider companies.
*Knowledge of antibacterial PK-PD. |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Director Clinical Research - Nexium/Lesogaberan |
| Requirements -- Education and Experience
* Graduate of a recognized school of medicine with an M.D. degree or equivalent.
* Specialty training and board certification in Internal Medicine or General Pediatrics and/or Gastroenterology
* Prior clinical experience and strong academic track record in gastrointestinal disease
* Three or more years of Drug Development experience obtained while working in the pharmaceutical industry with focus and expertise in gastrointestinal disease required for Director level position or equivalent strong Academic credentials with Industry related experience (Advisory Boards, Regulatory consultancy, participation in clinical trials, etc).
* Experience in designing, monitoring and implementing clinical trials and interpreting trial results, including basic understanding of biostatistics and safety reporting
* An understanding of pharmaceutical industry R&D, particularly of major clinical milestones and of the factors which influence those decision points
* An understanding of the interplay between clinical development and commercial objectives |
| AstraZeneca Pharmaceuticals |
Waltham |
MA |
9/4/2010
|
| In Vivo Scientist |
| *BS/MS degree in Pharmacology, Molecular Biology, Biochemistry, or equivalent with 10+ years of experience for the Scientist and 3 -- 10 years experience for the Senior Associate Scientist in animal models of human diseases, preferably in industrial oncology drug discovery.
*Experience in handling and dosing of rodents and formulation of test compounds is critical.
*Experience with basic molecular and cellular biology techniques, and with sterile tissue culture is required. Familiarity with advance models of cancer including surgical skills, orthotopic, metastatic, and host tumor model systems would be an advantage.
*Familiarity with Excel, Word, Power Point and graphics applications, as well as excellent writing, communication, and inter-personal skills are very important |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Dir Clinical Research - Onglyza |
| Requirements -- Education and Experience:
* Graduate of a recognized school of medicine with an M.D. degree or equivalent.
* Specialty training and board certification in Internal Medicine; Endocrinology; Diabetes and Metabolism; or Cardiovascular Medicine
* Three or more years of Drug Development experience obtained while working in the pharmaceutical industry with focus and expertise in metabolic disorders and diabetes.
* Prior clinical experience and strong academic track record in metabolic disorders and diabetes required
* Experience in designing, monitoring and implementing clinical trials and interpreting trial results, including understanding of biostatistics and safety reporting
* An understanding of pharmaceutical industry R&D, particularly of major clinical milestones and of the factors which influence those decision points.
* An understanding of the interplay between clinical development and commercial objectives
Organizational Behavior
1. Passion for Customer Solutions: Understands one's customers and uses that insight to provide value
2. Thinks Strategically: Quickly identifies and acts on opportunities, combining forethought with action. This is based on an understanding of the external environment and its impact on AZ
3. Acts Decisively: Makes and acts on decisions quickly and effectively and fosters the same in others. This is based on an underlying courage to enable risk-taking for the business
4. Drives Performance: Holds self and others accountable for the achievement of performance expectations. Creates an environment that enables others to perform at their best
5. Works Collaboratively: Actively creates and promotes cross-boundary collaboration with the aim of achieving better business results. Boundaries can exist between individuals, geographies, cultures, teams, functions, organizations
6. Develops People and Organization: Demonstrates a genuine commitment to the time and effort needed to develop oneself and others |
| AstraZeneca Pharmaceuticals |
Las Vegas |
NV |
9/4/2010
|
| Pharmaceutical Sales Specialist - CNS SC1 - Las Vegas E; N |
|
| AstraZeneca Pharmaceuticals |
New Orleans |
LA |
9/4/2010
|
| Pharmaceuticals Sales Specialist - CNSO - New Orleans; LA |
| EXPERIENCE:
*At least two years of documented, full-time, successful pharmaceutical sales, or at the discretion of those involved in the hiring process, related sales to physicians and hospitals such as medical equipment; or five years of experience in treating patients with CNS disorders, or in another CNS related business discipline.
*Experience and knowledge of CNS products and disorders, especially those associated in treating the chronic mentally ill.
*Experience selling and knowledge of CNS products or diseases preferred
*Experience selling in retail and non-retail settings including mental health clinics, hospitals, and office-based private practices.
*History of building and influencing customer relationships, and goal achievement
*Demonstrated clinical selling skills
*Demonstrated ability to manage PREP budget and to work through the PRA process
EDUCATION:
*Bachelors degree |
| AstraZeneca Pharmaceuticals |
Houston SE/SW |
TX |
9/4/2010
|
| Pharmaceuticals Sales Specialist - MCR - Houston /SW; TX Richmond/Sugarland/Rosenburg/Lake Jackson |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Jacksonville |
FL |
9/4/2010
|
| Pharmaceuticals Sales Specialist - CNSO - Jacksonville; FL |
| EXPERIENCE:
*At least two years of documented, full-time, successful pharmaceutical sales, or at the discretion of those involved in the hiring process, related sales to physicians and hospitals such as medical equipment; or five years of experience in treating patients with CNS disorders, or in another CNS related business discipline.
*Experience and knowledge of CNS products and disorders, especially those associated in treating the chronic mentally ill.
*Experience selling and knowledge of CNS products or diseases preferred
*Experience selling in retail and non-retail settings including mental health clinics, hospitals, and office-based private practices.
*History of building and influencing customer relationships, and goal achievement
*Demonstrated clinical selling skills
*Demonstrated ability to manage PREP budget and to work through the PRA process |
| AstraZeneca Pharmaceuticals |
Tacoma |
WA |
9/4/2010
|
| Pharmaceuticals Sales Specialist - MCL - Tacoma E; WA |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Southern |
IL |
9/4/2010
|
| Pharmaceutical Sales Specialist - Hospital - Southern IL |
| EDUCATION:
Bachelor's degree
EXPERIENCE:
At least two years of documented, full-time, successful pharmaceutical sales, or at the discretion of those involved in the hiring process, related sales to physicians and hospitals such as medical equipment; or five years of experience in treating patients with CNS disorders, or in another CNS related business discipline.
Experience and knowledge of CNS products and disorders, especially those associated in treating the chronic mentally ill.
Experience selling and knowledge of CNS products or diseases preferred
Experience selling in retail and non-retail settings including mental health clinics, hospitals, and office-based private practices.
History of building and influencing customer relationships, and goal achievement
Demonstrated clinical selling skills
Demonstrated ability to manage PREP budget and to work through the PRA process
ADDITIONAL SKILLS:
Knowledge of medical office equipment, territory management direct and in-direct sales processes
Possess excellent written and verbal communications skills, and presentation skills
Problem solving skills
Business administration skills
Laptop computer skills
Managed Care knowledge including prior authorization successes, demonstrated understanding of managed care contracting
Proven ability to understand, internalize, and routinely present challenging scientific information
Ability to freely accept, implement, and exchange best practices.
No Company relocation assistance will be provided. |
| AstraZeneca Pharmaceuticals |
Waltham |
MA |
9/4/2010
|
| Business Development Manager |
| Qualifications:
- Will have a BS/BA in a relevant scientific discipline and usually a second degree in a relevant scientific or business discipline
- Will have a strong knowledge of scientific principles guiding the aspects of diagnostics development
- Broad background across the diagnostic industry
- Experience in a Business Development role primarily in diagnostic / biotechnology industry
- Significant project management experience and ability to handle multiple projects
- Preferred deal negotiation experience
- Experience working globally preferred |
| AstraZeneca Pharmaceuticals |
Knoxville |
TN |
9/4/2010
|
| Pharmaceuticals Sales Specialist - MCL- Knoxville SW; TN |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Covington |
LA |
9/4/2010
|
| Pharmaceuticals Sales Specialist -MCL - Covington; LA |
| Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Pasadena |
TX |
9/4/2010
|
| Pharmaceuticals Sales Specialist - MCL - Pasadena; TX |
|
| AstraZeneca Pharmaceuticals |
Beaumont |
TX |
9/4/2010
|
| Pharmaceuticals Sales Specialist - MCL - Beaumont; TX |
|
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Associate Director Clinical Research- Respiratory/Inflammation TA |
| Graduate of a recognized school of medicine with an M.D. degree or equivalent.- Specialty training and board certification or eligibility in Pulmonology or Allergy.- Familiarity with biostatistics. Demonstrated clinical research experience in an academia or industry.- Excellent written and oral communication, interpersonal, and organizational skills.- Ability to travel nationally and internationally.
Preferred Background: Board eligibility/certification in Pulmonology or Allergy.- Background in clinical or basic science/translational research required. Five years or more experience in drug development/medical affairs required. Experience working with regulatory authorities, preparing regulatory documents, and preparation of promotional materials required. A thorough understanding of US pharmaceutical safety reporting and surveillance required. Experience supervising physicians and/or scientific staff in a management or team leader capacity highly desirable. Individuals with less experience may be considered for a Director level role.
Leadership Capabilities:
* Passion for Customers
* Thinks Strategically
* Acts Decisively
* Drives Performance
* Works Collaboratively
* Develops People & Organization |
| AstraZeneca Pharmaceuticals |
Bridgeport |
CT |
9/4/2010
|
| Pharmaceuticals Sales Specialist - MCL - Bridgeport; CT |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Director Clinical Research - Respiratory/Inflammation TA |
| Leadership Capabilities:
* Passion for Customers
* Thinks Strategically
* Acts Decisively
* Drives Performance
Graduate of a recognized school of medicine with an M.D. degree or equivalent.- Specialty training and board certification or eligibility in Pulmonology or Allergy.- Familiarity with biostatistics. Demonstrated clinical research experience in an academia or industry.- Excellent written and oral communication, interpersonal, and organizational skills.- Ability to travel nationally and internationally.
Preferred Background: Board eligibility/certification in Pulmonology or Allergy.- Background in clinical or basic science/translational research desirable. Two to three years experience in drug development/medical affairs (required for Director). Knowledge of CDER regulations regarding evaluation and approval of pharmaceuticals (regulatory interaction experience required for Director). An understanding of US pharmaceutical safety reporting and surveillance (required for Director).
Individuals with less experience may be considered for an Associate Director level role.
Leadership Capabilities:
* Works Collaboratively
* Develops People & Organization |
| AstraZeneca Pharmaceuticals |
Manhattan |
NY |
9/4/2010
|
| Pharmaceuticals Sales Specialist - MCL - Manhattan North; NY |
|
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Senior Safety Medical Director - Cardiac |
| Requirements --Education and Experience
Given the breadth of roles encompassed by this opportunity, it is recognized that some requirements may be more relevant to certain specific positions and, therefore, the following criteria are intended as guidance:
* Specialty training and board certified/eligible in cardiology/cardiovascular disease
* MD background with strong expertise in cardiology, ideally drug-induced cardiac injury.
* > 5 years of drug development/safety experience the majority of which should be in industry with clear evidence of delivery
* UK physicians will be expected to have completed Higher Medical Training in Pharmaceutical Medicine
* Recognized by peers for therapeutic area expertise and commercial/safety understanding
* Experience in supervising physicians
* Ability to balance business and clinical research objectives
* Experience working with regulatory agencies, preparing regulatory documents and overseeing submissions.
* A thorough knowledge of the pharmaceutical industry, especially clinical research and global regulatory requirements and practices governing expedited and periodic safety reporting, signal generation, safety evaluation and risk management activities
* Proven high quality scientific record
* Demonstrated capability to lead implementation of new technology and/or working routines within a complex organization.
* Excellent verbal and written communication skills.
* Experience in leading of cross-functional teams.
* Broad knowledge of drug development.
Skills and Capabilities
* Strong team-working skills and an ability to work collaboratively in a global pharmaceutical environment
* Strategic thinking
* Strategic influencing
Organizational Behaviors
* Foster behaviors that reinforce AZ as a global organization
* Ensure respect for different practices and expertise in different environments
* Ensure inclusivity of appropriate medical and scientific expertise in strategic and tactical decision-making
* Ensure medical/scientific integrity and commitment to effective communications
Reporting Relationship
* If applicable, this section contains a list of positions that report to the position, either directly or indirectly
* Reports -- none |
| AstraZeneca Pharmaceuticals |
San Diego S |
CA |
9/4/2010
|
| Pharmaceuticals Sales Specialist - MCL - San Diego S; CA |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Columbus NW |
OH |
9/4/2010
|
| Pharmaceuticals Sales Specialist - MCRO - Columbus NW; OH |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
- Function independently with a high degree of sales proficiency.
- Develop superior product and disease state knowledge and effectively educate and engage healthcare professionals in dialogue about clinical evidence, approved indications, and product efficacy/safety profiles to support on-label prescribing for appropriate patients.
- Drive sales performance and ensure sales forecasts and assigned budgets meet or exceed therapeutic and territory expectations.
- Achieve and exceed sales goals while managing a budget using good judgment.
- Successfully complete all training requirements, including product examinations.
- Regularly use a variety of analytical tools to understand and evaluate the business in order to best determine how to accomplish sales objectives.
- Develop and maintain in-depth knowledge of market, demographic, and managed care information relative to assigned sales territory.
- Work with Regional Sales Director and District Sales Manager to develop a local strategy and business plan to generate recognizable increases of sales in territory.
- Capitalize on formulary approvals and other opportunities through effective implementation of the Strategic Targeting Plan.
- Use a wide variety of promotional resources, analytical tools, and resource personnel to maximize effectiveness in assigned sales territory, based on local assessment of customer needs.
- Provide special education to healthcare providers through appropriate programs that fall within AstraZeneca's ethical guidelines.
- Work with other Pharmaceutical Sales Specialists around common objectives to coordinate selling efforts.
- Provide timely and competent administrative management of work hours, sales call data, customer objectives, communication responses, synchronization, sample and expense reporting.
- Work within a framework of AstraZeneca's Leadership Capabilities.
AstraZeneca is a global leader in research, development and marketing of gastrointestinal (GI), oncology (ONC), anesthesia/pain management (PAIN), cardiovascular (CV), central nervous system (CNS) and respiratory (RESP) products. Leveraging our powerful science-based culture, strengthened R&D platforms, and enhanced worldwide marketing/sales assets; AstraZeneca has emerged as one of the leading pharmaceutical companies in the world.
If you are interested in being considered for opportunities with AstraZeneca, please go to the following website:
http://www.AstraZenecaCareers.com
click on the 'Career Opportunities' link and then the 'career profile' link to complete the brief registration process. If you have already registered, you should have an ID and password to re-login and search for the requisition. Depending upon your qualifications and any existing opportunities, someone will contact you. If not, your information will be kept on file for future consideration.
AstraZeneca
Making a Difference
AstraZeneca is an equal opportunity employer |
| AstraZeneca Pharmaceuticals |
Utica |
NY |
9/4/2010
|
| Pharmaceutical Sales Specialist - HOSP - Utica; NY |
| Minimum Requirements
- Bachelor's Degree.
- Two years of pharmaceutical sales experience
- Strong clinical skill, and sales ability
- Internal candidate must be Career Ladder Level 2 and above
Skills and Competencies
- Effectively communicates complex clinical information
- Prioritizes tasks for greatest time efficiency
- Strong clinical aptitude, and the ability to sell in a clinical environment
- Ability to work collaboratively, with internal and external resource
- Ability to network in a hospital environment.
- Applies tactical thinking to overcome obstacles
- Ability to develop and leverage relationships with KOL, and key influencers
- Ability to set up speaker programs, CME programs and special events
Preferred Background
- Four or more years in AZ Pharmaceutical sales, or related sales experience, preferably in the anti-biotic, and respiratory markets
- Two or more years Hospital selling experience
- Experience influencing formulary decisions
- Experience working with MIS s |
| AstraZeneca Pharmaceuticals |
Charlotte |
NC |
9/4/2010
|
| Pharmaceuticals Sales Specialist - CNSO - Charlotte; NC |
| EXPERIENCE:
*At least two years of documented, full-time, successful pharmaceutical sales, or at the discretion of those involved in the hiring process, related sales to physicians and hospitals such as medical equipment; or five years of experience in treating patients with CNS disorders, or in another CNS related business discipline.
*Experience and knowledge of CNS products and disorders, especially those associated in treating the chronic mentally ill.
*Experience selling and knowledge of CNS products or diseases preferred
*Experience selling in retail and non-retail settings including mental health clinics, hospitals, and office-based private practices.
*History of building and influencing customer relationships, and goal achievement
*Demonstrated clinical selling skills
*Demonstrated ability to manage PREP budget and to work through the PRA process
EDUCATION:
*Bachelors degree |
| AstraZeneca Pharmaceuticals |
New Haven |
CT |
9/4/2010
|
| Pharmaceuticals Sales Specialist - MCL - New Haven; CT |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Lower Manhattan |
NY |
9/4/2010
|
| Pharmaceutical Sales Specialist - CNSO- Manhattan South; NY |
| EXPERIENCE:
*At least two years of documented, full-time, successful pharmaceutical sales, or at the discretion of those involved in the hiring process, related sales to physicians and hospitals such as medical equipment; or five years of experience in treating patients with CNS disorders, or in another CNS related business discipline.
*Experience and knowledge of CNS products and disorders, especially those associated in treating the chronic mentally ill.
*Experience selling and knowledge of CNS products or diseases preferred
*Experience selling in retail and non-retail settings including mental health clinics, hospitals, and office-based private practices.
*History of building and influencing customer relationships, and goal achievement
*Demonstrated clinical selling skills
*Demonstrated ability to manage PREP budget and to work through the PRA process
EDUCATION:
*Bachelors degree |
| AstraZeneca Pharmaceuticals |
New Bedford |
MA |
9/4/2010
|
| Pharmaceutical Sales Specialist - CNS SC1 - New Bedford; MA |
| EDUCATION:
* Bachelors degree
EXPERIENCE:
* At least two years of documented, full-time, successful pharmaceutical sales, or at the discretion of those involved in the hiring process, related sales to physicians and hospitals such as medical equipment; or five years of experience in treating patients with CNS disorders, or in another CNS related business discipline.
* Experience and knowledge of CNS products and disorders, especially those associated in treating the chronic mentally ill.
* Experience selling and knowledge of CNS products or diseases preferred
* Experience selling in retail and non-retail settings including mental health clinics, hospitals, and office-based private practices.
* History of building and influencing customer relationships, and goal achievement
* Demonstrated clinical selling skills
* Demonstrated ability to manage PREP budget and to work through the PRA process
ADDITIONAL SKILLS:
* Knowledge of medical equipment, territory management direct and in-direct sales processes
* Possess excellent written and verbal communications skills, and presentation skills
* Problem solving skills
* Business administration skills
* Laptop computer skills
* Managed Care knowledge including prior authorization successes, demonstrated understanding of managed care contracting
* Proven ability to understand, internalize, and routinely present challenging scientific information
* Ability to freely accept, implement, and exchange best practices
COMPANY:
AstraZeneca is a global leader in the research, development and marketing of gastrointestinal (GI), oncology (ONC), anesthesia/pain management (PAIN), cardiovascular (CV), central nervous system (CNS) and respiratory (RESP) products. Leveraging our powerful science-based culture, strengthened R&D platforms, and enhanced worldwide marketing/sales assets; AstraZeneca has emerged as one of the leading pharmaceutical companies in the world.
If you are interested in being considered for opportunities with AstraZeneca, please go to the following web site:
http://www.AstraZenecaCareers.com
click on the 'Career Opportunities' link and then the 'career profile' link to complete that brief registration process. If you have already registered, you should have an ID and password to re-login and search for the requisition. Depending upon your qualifications and any existing opportunities, someone will contact you. If not, your information will be kept on file for future consideration.
AstraZeneca
Making a Difference
AstraZeneca is an equal opportunity employer |
| AstraZeneca Pharmaceuticals |
Bronx |
NY |
9/4/2010
|
| Pharmaceuticals Sales Specialist - CNS SC1 - Manhattan - Bronx; NY |
| EDUCATION:
* Bachelors degree
EXPERIENCE:
* At least two years of documented, full-time, successful pharmaceutical sales, or at the discretion of those involved in the hiring process, related sales to physicians and hospitals such as medical equipment; or five years of experience in treating patients with CNS disorders, or in another CNS related business discipline.
* Experience and knowledge of CNS products and disorders, especially those associated in treating the chronic mentally ill.
* Experience selling and knowledge of CNS products or diseases preferred
* Experience selling in retail and non-retail settings including mental health clinics, hospitals, and office-based private practices.
* History of building and influencing customer relationships, and goal achievement
* Demonstrated clinical selling skills
* Demonstrated ability to manage PREP budget and to work through the PRA process
ADDITIONAL SKILLS:
* Knowledge of medical equipment, territory management direct and in-direct sales processes
* Possess excellent written and verbal communications skills, and presentation skills
* Problem solving skills
* Business administration skills
* Laptop computer skills
* Managed Care knowledge including prior authorization successes, demonstrated understanding of managed care contracting
* Proven ability to understand, internalize, and routinely present challenging scientific information
* Ability to freely accept, implement, and exchange best practices
COMPANY:
AstraZeneca is a global leader in the research, development and marketing of gastrointestinal (GI), oncology (ONC), anesthesia/pain management (PAIN), cardiovascular (CV), central nervous system (CNS) and respiratory (RESP) products. Leveraging our powerful science-based culture, strengthened R&D platforms, and enhanced worldwide marketing/sales assets; AstraZeneca has emerged as one of the leading pharmaceutical companies in the world.
If you are interested in being considered for opportunities with AstraZeneca, please go to the following web site:
http://www.AstraZenecaCareers.com
click on the 'Career Opportunities' link and then the 'career profile' link to complete that brief registration process. If you have already registered, you should have an ID and password to re-login and search for the requisition. Depending upon your qualifications and any existing opportunities, someone will contact you. If not, your information will be kept on file for future consideration.
AstraZeneca
Making a Difference
AstraZeneca is an equal opportunity employer |
| AstraZeneca Pharmaceuticals |
Waltham |
MA |
9/4/2010
|
| TA Medical Scientist-Oncology |
| Minimum Requirements --Education and Experience
* Relevant Clinical or Biomedical Ph.D or relevant Pharmacy, Msc/Mres degree with significant R&D experience
* 3-5 years of clinical drug development or medical affairs experience within a pharmaceutical company environment
* A degree of specialist knowledge of the medical and scientific activities related to a particular therapeutic area/indication and/or to an assigned project or product
* A good understanding of more than one development function
Skills and Capabilities
Leadership Capabilities- Level 2
* Passion for Customers
* Thinks Strategically
* Acts Decisively
* Drives Performance
* Works Collaboratively
* Develops People and Organizations
Additional Skills and Capabilities
* General Scientific & Medical understanding
* Ability to acquire and assimilate knowledge in different disciplines, disease and therapeutic areas
* Ability to credibly influence whilst maintaining independent and objective views
* Communication, interpersonal and organizational skills
* Attention to detail
* Analytical thinking
* Cultural awareness
* Commercial acumen
Internal and External customers/contacts
* Clinical Partnerships
* Investigators and KOLs
* Clinical Development functions eg., patient safety, regulatory,
* Clinical Biomarker Group
* Global Marketing, ISMO and marketing companies
* Discovery/Translational Science
Reporting Relationship
* Reports to GD or TACD |
| AstraZeneca Pharmaceuticals |
Waltham |
MA |
9/4/2010
|
| Associate Director DMPK (In Vitro) |
| Minimum Requirements:
· Ph.D. in a DMPK-related field plus at least 8 years experience in the pharmaceutical industry and in the DMPK discipline
· Experience in representing the DMPK discipline on cross-functional drug discovery project teams
· Demonstrated ability to influence, mentor and manage staff working toward project progression and candidate delivery
· Thorough knowledge of the DMPK discipline and a successful track record of the application of DMPK principles to drug discovery
· Proven ability to develop and enhance a DMPK area of specialism
· Familiarity with DMPK-related lead identification and optimization techniques
· Familiarity with and commitment to the pragmatic application of DMPK data to the optimization of lead compounds
Skills and Competencies:
· Strong leadership attributes and ability to leverage maximum potential from DMPK staff and to influence cross-functional drug discovery project team members
· Excellent team player and ability to work effectively with a variety of personalities
· Breadth and depth of knowledge of the DMPK discipline as it applies to the discovery and selection of high quality candidate drugs
· Strong scientific, strategic and organizational competency in discipline
· Breadth of knowledge and experience in the drug discovery arena
· Demonstrated ability to critically evaluate drug discovery problems and apply physico-chemical and DMPK tools and principles to achieve solutions
· Ability to martial and apply multi-disciplinary resources to achieve drug discovery goals
· Developed expertise in a specific sub-discipline of DMPK with the ability to communicate and apply this expertise to drug discovery challenges
· A focus on speed and delivery while maintaining quality of results
· Excellent verbal and written communication skills
Preferred Background:
· Expertise in the principles of DMPK, in the application of experimental techniques to optimize and characterize the disposition of drugs and in managing senior level staff |
| AstraZeneca Pharmaceuticals |
Hartford |
CT |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Hartford North, CT |
| Qualifications:
Education:
-Bachelors degree (any major) from an accredited college or university is required. |
| AstraZeneca Pharmaceuticals |
Lower Manhattan |
NY |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Upper Manhattan East, NY |
| Qualifications:
Education:
-Bachelors degree (any major) from an accredited college or university is required. |
| AstraZeneca Pharmaceuticals |
Columbus NE |
OH |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Columbus Metro, OH |
| Qualifications:
Education:
-Bachelors degree (any major) from an accredited college or university is required. |
| AstraZeneca Pharmaceuticals |
Hattisburg |
MS |
9/4/2010
|
| Pharmaceutical Sales Representative- MCL - Hattisbug,MS |
| Qualifications:
Education:
-Bachelors degree (any major) from an accredited college or university is required. |
| AstraZeneca Pharmaceuticals |
Birmingham SW |
AL |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Birmingham S, AL |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Riverdale |
GA |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Riverdale, GA |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Bakersfield |
CA |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Bakersfield, CA |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Tupelo |
MS |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Tupelo, MS |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Cincinnati E |
OH |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Cincinnati E, OH |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Brockton |
MA |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Brockton, MA |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Raleigh |
NC |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Raleigh E, NC |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Kissimmee |
FL |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Kissemmee, FL |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Red Bank |
NJ |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Red Bank, NJ |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Hawaii |
HI |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Hawaii N, HI |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Huntsville |
AL |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Hunstville, AL |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Pikeville |
KY |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Pikeville, KY |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
San Diego N |
CA |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - San Diego W, CA |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Plano |
TX |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Plano, TX |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
State College |
PA |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - State College, PA |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Pensacola |
FL |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Pensacola, FL |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
White Plains |
NY |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - White Plains, NY |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Asheville |
NC |
9/4/2010
|
| Pharmaceutical Sales Specialist - Hospital Care Team - Asheville, NC |
| EXPERIENCE:
*At least three years of documented, successful pharmaceutical sales, or at the discretion of those involved in the hiring process, related sales to physicians and hospitals such as medical equipment.
*Experience selling and knowledge of products/diseases within one or more therapeutic areas: CNS and Respiratory
*Experience selling in a Hospital or large account setting
*History of building and influencing customer relationships, and goal achievement
*Demonstrated clinical selling skills
*Demonstrated ability to manage PREP budget and to work through the PRA process
EDUCATION:
*Bachelors degree |
| AstraZeneca Pharmaceuticals |
Jackson S |
MS |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Jackson S, MS |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Hagerstown |
MD |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Hagerstown, MD |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Los Angeles South |
CA |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCLO - Los Angeles S, CA |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Merced |
CA |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Merced, CA |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Warwick |
RI |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Warwick, RI |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Savannah |
GA |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Savannah, GA |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Jersey City |
NJ |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCLO - Jersey City, NJ |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Boca Raton |
FL |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Boca Raton, FL |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Ventura |
CA |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Ventura, CA |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
San Antonio E |
TX |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - San Antonio E, TX |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Syracuse |
NY |
9/4/2010
|
| Pharmaceutical Sales Specialist - CNS SC2 - Syracuse; NY |
| EDUCATION:
* Bachelors degree
EXPERIENCE:
* At least two years of documented, full-time, successful pharmaceutical sales, or at the discretion of those involved in the hiring process, related sales to physicians and hospitals such as medical equipment; or five years of experience in treating patients with CNS disorders, or in another CNS related business discipline.
* Experience and knowledge of CNS products and disorders, especially those associated in treating the chronic mentally ill.
* Experience selling and knowledge of CNS products or diseases preferred
* Experience selling in retail and non-retail settings including mental health clinics, hospitals, and office-based private practices.
* History of building and influencing customer relationships, and goal achievement
* Demonstrated clinical selling skills
* Demonstrated ability to manage PREP budget and to work through the PRA process
ADDITIONAL SKILLS:
* Knowledge of medical equipment, territory management direct and in-direct sales processes
* Possess excellent written and verbal communications skills, and presentation skills
* Problem solving skills
* Business administration skills
* Laptop computer skills
* Managed Care knowledge including prior authorization successes, demonstrated understanding of managed care contracting
* Proven ability to understand, internalize, and routinely present challenging scientific information
* Ability to freely accept, implement, and exchange best practices
COMPANY:
AstraZeneca is a global leader in the research, development and marketing of gastrointestinal (GI), oncology (ONC), anesthesia/pain management (PAIN), cardiovascular (CV), central nervous system (CNS) and respiratory (RESP) products. Leveraging our powerful science-based culture, strengthened R&D platforms, and enhanced worldwide marketing/sales assets; AstraZeneca has emerged as one of the leading pharmaceutical companies in the world.
If you are interested in being considered for opportunities with AstraZeneca, please go to the following web site:
http://www.AstraZenecaCareers.com
click on the 'Career Opportunities' link and then the 'career profile' link to complete that brief registration process. If you have already registered, you should have an ID and password to re-login and search for the requisition. Depending upon your qualifications and any existing opportunities, someone will contact you. If not, your information will be kept on file for future consideration.
AstraZeneca
Making a Difference
AstraZeneca is an equal opportunity employer |
| AstraZeneca Pharmaceuticals |
Atlanta |
GA |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Atlanta E, GA |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Newark |
NJ |
9/4/2010
|
| Pharmaceutical Sales Specialist - CNS SC2 - Newark; NJ |
| EDUCATION:
* Bachelors degree
EXPERIENCE:
* At least two years of documented, full-time, successful pharmaceutical sales, or at the discretion of those involved in the hiring process, related sales to physicians and hospitals such as medical equipment; or five years of experience in treating patients with CNS disorders, or in another CNS related business discipline.
* Experience and knowledge of CNS products and disorders, especially those associated in treating the chronic mentally ill.
* Experience selling and knowledge of CNS products or diseases preferred
* Experience selling in retail and non-retail settings including mental health clinics, hospitals, and office-based private practices.
* History of building and influencing customer relationships, and goal achievement
* Demonstrated clinical selling skills
* Demonstrated ability to manage PREP budget and to work through the PRA process
ADDITIONAL SKILLS:
* Knowledge of medical equipment, territory management direct and in-direct sales processes
* Possess excellent written and verbal communications skills, and presentation skills
* Problem solving skills
* Business administration skills
* Laptop computer skills
* Managed Care knowledge including prior authorization successes, demonstrated understanding of managed care contracting
* Proven ability to understand, internalize, and routinely present challenging scientific information
* Ability to freely accept, implement, and exchange best practices |
| AstraZeneca Pharmaceuticals |
Birmingham |
AL |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Birmingham S, AL |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Woodbridge |
VA |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Woodbridge, VA |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Chicago |
IL |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Woodridge, IL |
| External Summary of Primary Responsibilities:
Responsibilities:
- Function independently with a high degree of sales proficiency.
- Develop superior product and disease state knowledge and effectively educate and engage healthcare professionals in dialogue about clinical evidence, approved indications, and product efficacy/safety profiles to support on-label prescribing for appropriate patients.
- Drive sales performance and ensure sales forecasts and assigned budgets meet or exceed therapeutic and territory expectations.
- Achieve and exceed sales goals while managing a budget using good judgment.
- Successfully complete all training requirements, including product examinations.
- Regularly use a variety of analytical tools to understand and evaluate the business in order to best determine how to accomplish sales objectives.
- Develop and maintain in-depth knowledge of market, demographic, and managed care information relative to assigned sales territory.
- Work with Regional Sales Director and District Sales Manager to develop a local strategy and business plan to generate recognizable increases of sales in territory.
- Capitalize on formulary approvals and other opportunities through effective implementation of the Strategic Targeting Plan.
- Use a wide variety of promotional resources, analytical tools, and resource personnel to maximize effectiveness in assigned sales territory, based on local assessment of customer needs.
- Provide special education to healthcare providers through appropriate programs that fall within AstraZeneca's ethical guidelines.
- Work with other Pharmaceutical Sales Specialists around common objectives to coordinate selling efforts.
- Provide timely and competent administrative management of work hours, sales call data, customer objectives, communication responses, synchronization, sample and expense reporting.
- Work within a framework of AstraZeneca's Leadership Capabilities.
AstraZeneca is a global leader in research, development and marketing of gastrointestinal (GI), oncology (ONC), anesthesia/pain management (PAIN), cardiovascular (CV), central nervous system (CNS) and respiratory (RESP) products. Leveraging our powerful science-based culture, strengthened R&D platforms, and enhanced worldwide marketing/sales assets; AstraZeneca has emerged as one of the leading pharmaceutical companies in the world.
If you are interested in being considered for opportunities with AstraZeneca, please go to the following website:
http://www.AstraZenecaCareers.com
click on the 'Career Opportunities' link and then the 'career profile' link to complete the brief registration process. If you have already registered, you should have an ID and password to re-login and search for the requisition. Depending upon your qualifications and any existing opportunities, someone will contact you. If not, your information will be kept on file for future consideration.
AstraZeneca
Making a Difference
AstraZeneca is an equal opportunity employer |
| AstraZeneca Pharmaceuticals |
Shreveport |
LA |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCLO - Shreveport; LA |
| External Summary of Primary Responsibilities:
Responsibilities:
- Function independently with a high degree of sales proficiency.
- Develop superior product and disease state knowledge and effectively educate and engage healthcare professionals in dialogue about clinical evidence, approved indications, and product efficacy/safety profiles to support on-label prescribing for appropriate patients.
- Drive sales performance and ensure sales forecasts and assigned budgets meet or exceed therapeutic and territory expectations.
- Achieve and exceed sales goals while managing a budget using good judgment.
- Successfully complete all training requirements, including product examinations.
- Regularly use a variety of analytical tools to understand and evaluate the business in order to best determine how to accomplish sales objectives.
- Develop and maintain in-depth knowledge of market, demographic, and managed care information relative to assigned sales territory.
- Work with Regional Sales Director and District Sales Manager to develop a local strategy and business plan to generate recognizable increases of sales in territory.
- Capitalize on formulary approvals and other opportunities through effective implementation of the Strategic Targeting Plan.
- Use a wide variety of promotional resources, analytical tools, and resource personnel to maximize effectiveness in assigned sales territory, based on local assessment of customer needs.
- Provide special education to healthcare providers through appropriate programs that fall within AstraZeneca's ethical guidelines.
- Work with other Pharmaceutical Sales Specialists around common objectives to coordinate selling efforts.
- Provide timely and competent administrative management of work hours, sales call data, customer objectives, communication responses, synchronization, sample and expense reporting.
- Work within a framework of AstraZeneca's Leadership Capabilities.
AstraZeneca is a global leader in research, development and marketing of gastrointestinal (GI), oncology (ONC), anesthesia/pain management (PAIN), cardiovascular (CV), central nervous system (CNS) and respiratory (RESP) products. Leveraging our powerful science-based culture, strengthened R&D platforms, and enhanced worldwide marketing/sales assets; AstraZeneca has emerged as one of the leading pharmaceutical companies in the world.
If you are interested in being considered for opportunities with AstraZeneca, please go to the following website:
http://www.AstraZenecaCareers.com
click on the 'Career Opportunities' link and then the 'career profile' link to complete the brief registration process. If you have already registered, you should have an ID and password to re-login and search for the requisition. Depending upon your qualifications and any existing opportunities, someone will contact you. If not, your information will be kept on file for future consideration.
AstraZeneca
Making a Difference
AstraZeneca is an equal opportunity employer |
| AstraZeneca Pharmaceuticals |
Midtown Manhattan |
NY |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Midtown East Side, NY |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Lincoln |
NE |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Lincoln, NE |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Waltham |
MA |
9/4/2010
|
| Associate/Senior Associate Scientist |
| Competencies (Knowledge/Skills):
* B.S., M.S. or equivalent in chemistry with 0-10 yrs of post-graduate experience.
* Knowledge and understanding of safe operating practices.
* Proficiency in experimental design. Experience in relevant methods and techniques.
* Skilled in theory and operation of lab equipment.
* Knowledge and understanding of database and analytical software.
* Rapidly adapts to new experimental approaches; acquires new skills and techniques readily. Develop understanding of how own work within the team supports the objectives of the project team and R&D discovery.
* Keeps own knowledge current regarding appropriate techniques and scientific advances in the work area. Presents data effectively at project and/or team meetings.
* Communicates relevant information from meetings or literature to colleagues.
* Communicates effectively with colleagues at all levels.
Behaviors:
Is reliable, has strong work ethic, and shows respect for colleagues. Willingly shares expertise and ideas. Is candid and honest in discussions. Demonstrates flexibility, open-mindedness, and adaptability. Has a 'can do attitude', maintains consistent work level despite negative results. Ensures productivity, quality, and timeliness. Commitment to team goals. Expands personal skills and knowledge as required to be effective. Act in accordance with all AstraZeneca policies on personnel, SHE, best laboratory practice, etc. |
| AstraZeneca Pharmaceuticals |
Florence |
SC |
9/4/2010
|
| Pharmaceutical Sales Specialist - CNS SC2 - Florence, SC |
| EXPERIENCE:
* At least two years of documented, full-time, successful pharmaceutical sales, or at the discretion of those involved in the hiring process, related sales to physicians and hospitals such as medical equipment; or five years of experience in treating patients with CNS disorders, or in another CNS related business discipline.
* Experience and knowledge of CNS products and disorders, especially those associated in treating the chronic mentally ill.
* Experience selling and knowledge of CNS products or diseases preferred
* Experience selling in retail and non-retail settings including mental health clinics, hospitals, and office-based private practices.
* History of building and influencing customer relationships, and goal achievement
* Demonstrated clinical selling skills
* Demonstrated ability to manage PREP budget and to work through the PRA process
ADDITIONAL SKILLS:
* Knowledge of medical equipment, territory management direct and in-direct sales processes
* Possess excellent written and verbal communications skills, and presentation skills
* Problem solving skills
* Business administration skills
* Laptop computer skills
* Managed Care knowledge including prior authorization successes, demonstrated understanding of managed care contracting
* Proven ability to understand, internalize, and routinely present challenging scientific information
* Ability to freely accept, implement, and exchange best practices |
| AstraZeneca Pharmaceuticals |
Worcester |
MA |
9/4/2010
|
| Pharmaceutical Sales Specialist - CNS SC2 - Worcester, MA |
| EXPERIENCE:
* At least two years of documented, full-time, successful pharmaceutical sales, or at the discretion of those involved in the hiring process, related sales to physicians and hospitals such as medical equipment; or five years of experience in treating patients with CNS disorders, or in another CNS related business discipline.
* Experience and knowledge of CNS products and disorders, especially those associated in treating the chronic mentally ill.
* Experience selling and knowledge of CNS products or diseases preferred
* Experience selling in retail and non-retail settings including mental health clinics, hospitals, and office-based private practices.
* History of building and influencing customer relationships, and goal achievement
* Demonstrated clinical selling skills
* Demonstrated ability to manage PREP budget and to work through the PRA process
ADDITIONAL SKILLS:
* Knowledge of medical equipment, territory management direct and in-direct sales processes
* Possess excellent written and verbal communications skills, and presentation skills
* Problem solving skills
* Business administration skills
* Laptop computer skills
* Managed Care knowledge including prior authorization successes, demonstrated understanding of managed care contracting
* Proven ability to understand, internalize, and routinely present challenging scientific information
* Ability to freely accept, implement, and exchange best practices |
| AstraZeneca Pharmaceuticals |
Miami Beach |
FL |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Miami Beach, FL |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Lafayette |
LA |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Lafayette, LA |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Clarksburg |
WV |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCLO - Clarksburg, WV |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Charleston |
WV |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCLO - Charleston, WV |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Gadsden |
AL |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Gadsden, AL |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Northridge |
CA |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCLO - Northridge, CA |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Binghamton |
NY |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCLO - Binghamton, NY |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Knoxville |
TN |
9/4/2010
|
| Pharmaceuticals Sales Specialist - MCL - Knoxville North; TN |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Lancaster |
PA |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Lancaster, PA |
| Qualifications:
Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Langhorne |
PA |
9/4/2010
|
| Pharmaceutical Sales Specialist - CNS SC2 - Langhorne, PA |
| EDUCATION:
* Bachelors degree
EXPERIENCE:
*At least two years of documented, full-time, successful pharmaceutical sales, or at the discretion of those involved in the hiring process, related sales to physicians and hospitals such as medical equipment; or five years of experience in treating patients with CNS disorders, or in another CNS related business discipline.
*Experience and knowledge of CNS products and disorders, especially those associated in treating the chronic mentally ill.
*Experience selling and knowledge of CNS products or diseases preferred
*Experience selling in retail and non-retail settings including mental health clinics, hospitals, and office-based private practices.
*History of building and influencing customer relationships, and goal achievement
*Demonstrated clinical selling skills
*Demonstrated ability to manage PREP budget and to work through the PRA process
ADDITIONAL SKILLS:
*Knowledge of medical equipment, territory management direct and in-direct sales processes
*Possess excellent written and verbal communications skills, and presentation skills
*Problem solving skills
*Business administration skills
*Laptop computer skills
*Managed Care knowledge including prior authorization successes, demonstrated understanding of managed care contracting
*Proven ability to understand, internalize, and routinely present challenging scientific information
*Ability to freely accept, implement, and exchange best practices
COMPANY:
AstraZeneca is a global leader in the research, development and marketing of gastrointestinal (GI), oncology (ONC), anesthesia/pain management (PAIN), cardiovascular (CV), central nervous system (CNS) and respiratory (RESP) products. Leveraging our powerful science-based culture, strengthened R&D platforms, and enhanced worldwide marketing/sales assets; AstraZeneca has emerged as one of the leading pharmaceutical companies in the world. |
| AstraZeneca Pharmaceuticals |
Fayetteville |
AR |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCLO - Fayetteville, AR |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Greenville |
NC |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Greenville, NC |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Omaha |
NE |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Omaha, NE |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Los Angeles |
CA |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCLO - Anaheim, CA |
| Responsibilities:
- Function independently with a high degree of sales proficiency.
- Develop superior product and disease state knowledge and effectively educate and engage healthcare professionals in dialogue about clinical evidence, approved indications, and product efficacy/safety profiles to support on-label prescribing for appropriate patients.
- Drive sales performance and ensure sales forecasts and assigned budgets meet or exceed therapeutic and territory expectations.
- Achieve and exceed sales goals while managing a budget using good judgment.
- Successfully complete all training requirements, including product examinations.
- Regularly use a variety of analytical tools to understand and evaluate the business in order to best determine how to accomplish sales objectives.
- Develop and maintain in-depth knowledge of market, demographic, and managed care information relative to assigned sales territory.
- Work with Regional Sales Director and District Sales Manager to develop a local strategy and business plan to generate recognizable increases of sales in territory.
- Capitalize on formulary approvals and other opportunities through effective implementation of the Strategic Targeting Plan.
- Use a wide variety of promotional resources, analytical tools, and resource personnel to maximize effectiveness in assigned sales territory, based on local assessment of customer needs.
- Provide special education to healthcare providers through appropriate programs that fall within AstraZeneca's ethical guidelines.
- Work with other Pharmaceutical Sales Specialists around common objectives to coordinate selling efforts.
- Provide timely and competent administrative management of work hours, sales call data, customer objectives, communication responses, synchronization, sample and expense reporting.
- Work within a framework of AstraZeneca's Leadership Capabilities.
AstraZeneca is a global leader in research, development and marketing of gastrointestinal (GI), oncology (ONC), anesthesia/pain management (PAIN), cardiovascular (CV), central nervous system (CNS) and respiratory (RESP) products. Leveraging our powerful science-based culture, strengthened R&D platforms, and enhanced worldwide marketing/sales assets; AstraZeneca has emerged as one of the leading pharmaceutical companies in the world. |
| AstraZeneca Pharmaceuticals |
Akron |
OH |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Akron N, OH |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Jackson N |
MS |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Jackson N, MS |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Los Angeles N |
CA |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Glendale, CA |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Executive Director Medical Science- Managed Markets |
| Minimum Requirements:
* Graduate of a recognized school of medicine with an M.D. degree and a current valid medical license. Medical board certification with demonstrated expertise in a field of medicine relevant to AstraZeneca's products
* A minimum of five years experience in managed care, such as a health plan or pharmacy benefit manager
* Experience in Drug Development at all levels and has a clear understanding of clinical trial development and implementation
* Experience in use of large databases for Pharmacoepi trial design or outcome assessments
* Broad medical knowledge base across disease areas and TA
* Leadership experience plus excellent written, oral communication, interpersonal, and organization skills
* Ability to develop and leverage professional relationships and a well-formed network of established contacts in MM area
* Proven teamwork and collaboration skills
* Ability to interact widely and effectively within the company (i.e., on an interdepartmental and interdisciplinary basis), and with AstraZeneca partners and Managed Markets customers
* Ability to travel nationally and internationally
* Familiarity with DDMAC promotional regulations, pharmaceutical promotion standards and federal and state anti-kickback laws
Preferred Background:
* Additional training in public health or business/health management, possession of an M.P.H., MBA or Ph.D. degree
* Professional and customer presentation experience and service orientation
* A well-formed network of established contacts in the assigned area
* Demonstrated understanding of the pharmaceutical industry, managed markets and the governmental dynamics affecting the industry
* Comprehensive understanding of broad business environment issues, pharmaceutical product development, product commercialization, and commercial portfolio planning issues
* Familiarity with FDA regulatory process for drug approval and other regulatory interactions ( e.g. sNDA, Pharmacovigilence) |
| AstraZeneca Pharmaceuticals |
Binghamton |
NY |
9/4/2010
|
| Pharmaceutical Sales Specialist - CNS SC1 - Binghamton, NY |
| EDUCATION:
* Bachelors degree
EXPERIENCE:
*At least two years of documented, full-time, successful pharmaceutical sales, or at the discretion of those involved in the hiring process, related sales to physicians and hospitals such as medical equipment; or five years of expe | |
