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| 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 |
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
|
| 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 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 |
| 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 Biostatistician |
| Typically requires a Master's Degree in Statistics with at least 3 years of related experience. Typical entry level with Ph.D. in Statistics. To be considered for this level, demonstrated proficiency in the following skills and responsibilities are required: With supervision, apply advanced statistical/programming and/or PK/PD modeling in the preparation of CSRs, manuscripts, ISSs, and ISEs that meet world-wide health authority and medical community standards, and participate in protocol preparation. |
| 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
|
| 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 |
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
|
| 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 |
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
|
| Associate Scientist - Molecular Diagnostics |
| Education:
The candidate must have a BS/MS degree in Life sciences (such as Molecular and Cell Biology, Genetics and Biochemistry) with 5+ years of lab experience.
Languages: English
Qualifications:
1. Hands-on experience on molecular biology techniques such as nucleic acid sample preparation, PCR, RT-PCR, gel electrophoresis, cloning, DNA sequencing, allele specific PCR, Real time PCR, melting curve analysis, SNP detection.
2. Working experience in tissue culture;
3. Familiarity with GLP and cGMP environment, documentation and quality system is highly desirable but not required.
4. General knowledge with basic statistics. Understanding the principles of DOE and hands-on experiences with statistics tools, Minitab or JMP, and bioinformatics tools as plus.
5. Good communication and time management skills. Good team player in multidisciplinary environment, capable of multiple tasking, and able to be fully committed to development timelines. |
| 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 |
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 |
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 |
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 |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Research Associate/ Senior Research Associate ? Molecular Biology - Agensys, Santa Monica, CA |
| The ideal candidate will have M.S. (preferred) or B.S. in Molecular Biology or related field, with a minimum of five (5) years of relevant research experience. Experience in molecular biology techniques and methods, with emphasis on gene expression and gene structure analysis is required. The ability to reliably handle and process precious and limited specimens is essential. Excellent verbal and written communication skills, as well as the ability to work both independently and in a team environment are required. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Director, Translational Research - Agensys, Santa Monica, CA |
| Candidate consideration requires a Ph.D./M.D. with a minimum of 10 years of post-doctoral experience. Industrial experience in Oncology drug discovery and experience managing scientists is required. Successful candidates will have strong written and oral communication skills, be self-motivated, demonstrate leadership and possess an exemplary record of research, as evidenced by publications and patents. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Associate Biostatistics Director, Oncology |
| M.S. or Ph.D. in statistics or equivalentRequired proven oncology experience Minimum of 8 years experience in applying statistical methods in biomedical research, extensive pharmaceutical or CRO experience requiredExperience in working on clinical project teams. Good understanding of entire drug development process - ability to see the ?big picture?.Experience as the independent lead statistician in a regulatory submission preferredExperience with cross functional process improvement or innovation initiativesAdvanced and broad knowledge of statistical methods, along with understanding of industry practices related to the statistical analysis of clinical dataKnowledge and skills in SAS required and knowledge of other statistical software preferred.In-depth familiarity with processes and procedures in data management and SAS programmingExperience working in an international environment and demonstrated ability to manage and influence across different locations, time zones and cultures; builds global relationships. Ability to work in a matrix environment. Proven excellent organizational, project and time management skills.Leadership skills and ability to delegate appropriately and provide direction to more junior Biostatisticians. Very good oral, written, and presentation communication skills. Able to clearly communicate statistical issues and methods to both statisticians and non-statisticians. Very good problem solving skills.Accurate with a keen eye for detail. Dedication to quality and reliability in all work tasksAbility to perform under pressure |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Associate Director, HEOR Biostatistics |
Education/Experience Qualified candidates must have an advanced degree in biostatistics or relevant field and a minimum of 5 years experience in the pharmaceutical industry or consulting organization. Ph.D. is preferred. Analytical experience in cardiovascular and oncology; and knowledge of cardiovascular and oncology therapeutic areas is preferred. Proficiency in data management across multiple platforms; expertise in using statistical software such as SAS and SPSS; and scientific computer programming, database querying, and descriptive and inferential statistics are required. Experience with economic modeling, multiple imputation techniques and truncated data analysis is preferred. Must be willing to travel 10% of the time. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Exec. Medical Dir Medical Research TA Head - Oncology |
Education/Experience Qualified candidates must have a MD degree with a minimum of 10 years experience in oncology clinical, research or academic medicine and either a minimum of 7 years of pharmaceutical industry experience or 15 years experience in academic medicine with experience conducting industry sponsored trials. Experience with oncology medical strategies and clinical trial implementations are required. Leadership experience managing scientific staff is required. Subspecialty training in the area of oncology is highly desired. Experience in the business development area would be a plus. Excellent written and oral communication skills, particularly strong formal presentation skills; strong interpersonal skills commensurate with the need to work closely with outside physicians/ scientists and numerous in-house support groups; knowledge of scientific methods, research design and medical practices and procedures that would be acquired through clinical experience and clinical research studies; good understanding of the current legal and regulatory environment are critical skills in this role. Basic knowledge and appropriate application of biostatistics is required in this role. Must be willing to travel up to 40% with up to 10% international travel. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Exec. Medical Dir Medical Research TA Head - Hypertension & Metabolism |
Education/Experience Qualified candidates must have a MD degree with a minimum of 10 years experience in clinical, research or academic medicine and a minimum of 7 years of pharmaceutical industry experience; leadership experience managing scientific staff; and experience with cardiovascular medical strategies and clinical trial implementations. Advanced training in cardiovascular medicine is highly desired. Experience in the business development area would be a plus. Excellent written and oral communication skills, particularly strong formal presentation skills; strong interpersonal skills commensurate with the need to work closely with outside physicians/ scientists and numerous in-house support groups; knowledge of scientific methods, research design and medical practices and procedures that would be acquired through clinical experience and clinical research studies; good understanding of the current legal and regulatory environment are critical skills in this role. Basic knowledge and appropriate application of biostatistics is required in this role. Additional training in the area of cardiovascular medicine is highly desired; experience with hypertension and metabolism products are required Must be willing to travel up to 40% with up to 10% international travel. |
| Daiichi Sankyo, Inc. |
Edison |
NJ |
9/3/2010
|
| Manager, Medical Writing |
Education/Experience Qualified candidates must have a PharmD, PhD in biological sciences. MD is strongly preferred. Otherwise exceptional candidates with a MS or BS/BA may be considered. Minimum requirement of 3 years experience with PharmD or PhD, 5 years with Masters’ Degree or 7 years with a BA/BS. Experience in writing regulatory documents (protocols, Investigator Brochures [IBs], Clinical Study Reports (CSRs), clinical sections of the CTD [2.5, 2.7.3, 2.7.4], integrated summaries of efficacy and safety [ISE and ISS], briefing books, and regulatory responses) in the pharmaceutical or CRO environment required; ability to interpret and organize scientific data; and general understanding of clinical research, biostatistics, electronic publishing, and relevant industry guidelines (GCP, eCTD, and ICH). Marketing submission experience (NDAs or MAAs) preferred but not required. Daiichi Sankyo develops or has developed drugs in the following therapeutic areas: cardiovascular diseases, metabolic diseases, inflammation and immunology, infectious diseases, and oncology. Relevant therapeutic area experience preferred. Ability to quickly get up to speed on a therapeutic area, project, or indication with little to no coaching, work concurrently on several complex projects, meet aggressive deadlines, and adjust priorities rapidly as the situation demands. Strong interpersonal and communication skills (both verbal and written) are also required as the individual must be able to work in a team environment and coordinate with the team to move documents forward to completion. Must be a self-motivated person who can work with limited guidance/supervision. Excellent writing skills with a clear concise style and excellent grammar, punctuation, and spelling; proficiency in a Microsoft Windows environment; and strong MS Word skills and ability to work with templates. Excellent attention to details, especially as related to accuracy of numbers/statements and consistency within and across documents. |
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Clinical Research Manager II |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Medical Director |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Clinical Research Manager II |
|
| New England Biolabs, Inc. (NEB) |
Ipswich |
MA |
9/3/2010
|
| Postdoctoral Fellowship – Bioinformatics |
| Qualifications:
•Ph.D. in computational biology or related field.
•A strong record of scientific publication.
•Creative data visualization skills.
•A positive attitude and a strong work ethic.
This position offers exciting opportunities for broad research training, collaboration with academic institutions, publishing in peer-reviewed journals and participation in national and international conferences.
New England Biolabs, Inc. is an equal opportunity employer M/F/D/V
|
| HireLifeScience.com |
Somerset |
NJ |
9/4/2010
|
| The HireLifeScience.com Career Fair - 9/21/10 |
| Required qualifications to attend:
Candidates must possess a 4 year life science related degree and 2 years professional experience working for a Life Science related company. You may pre-register at http://career.hirelifescience.com/ An invitation to attend will be sent if the minimum qualifications are met. |
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