| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Director Field Medical Physician (CV) |
· Graduate of a recognized medical school and recipient of an M.D. degree
· Range of 11 - 33 years of clinical practice
· Board certification in cardiology
· Background in academic medicine, clinical research, and familiarity with biostatistics
· Excellent written and oral communication, interpersonal, and organization skills
· Demonstrated ability to proactively and positively engage teams through multiple communications channels including telephone, e-mail, Internet, and face-to-face
· Ability to travel nationally and internationally
Preferred Background
· Other training such as an M.P.H. or other advanced degree
· Experience with or business acumen around working within the pharmaceutical industry
· Experience with pharmaceutical drug development and medical/scientific affairs
· National recognition as a key opinion leader as demonstrated by a track record of scholarship, independent research funding, publications, and membership in national societies
· Familiarity with DDMAC, PhRMA code, and key regulations in the pharmaceutical industry
· Geographically located close to Wilmington, Delaware headquarters
 |
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Director Clinical Research- Early Development Neuroscience TA |
| Minimum Requirements:- Graduate of a recognized school of medicine with an M.D. degree or equivalent.- Specialty training and board certification or eligibility in Psychiatry or Neurology.- Familiarity with biostatistics.- Excellent written and oral communication, interpersonal, and organizational skills.- Ability to travel nationally and internationally.Preferred Background:- Board certification in Psychiatry or Neurology.- Scientific training such as a Ph.D. degree is desirable.- Three to five years experience in drug development/medical affairs (Director).- Knowledge of CDER regulations regarding evaluation and approval of pharmaceuticals (Director).- An understanding of US pharmaceutical safety reporting and surveillance.
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Director**- Clinical Research- Brilinta Brand Team |
| 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; Specialty Certificationin Cardiovascular Medicine highly desireable.
· Three or more years of Drug Development experience obtained while working in the pharmaceutical industry with focus and expertise in cardiovascular disease especially in the area of thrombosis. Exceptionally well qualified candidates without prior pharmaceutical company experience may be considered.
· Prior clinical experience and strong academic track record in cardiovascular disease required.
· Experience in designing, monitoring and implementing clinical trials and interpreting trial results, including understanding of biostatistics, safety reporting, and regulatory requirements
· 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.
· Excellent presentation skills.
** Please note: Depending on experience, this role may be modified to that of the Associate Direrctor or Senior Director level.
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Director** Clinical Research- Crestor/Certriad Brand Team |
| · Graduate of a recognized school of medicine with an M.D. degree or equivalent.
· · Specialty training and board certification in Internal Medicine; Pediatrics (with appropriate subspecialty); Endocrinology; Diabetes and Metabolism; or Cardiovascular Medicine .
· Three or more years of Drug Development experience obtained while working in the pharmaceutical industry for Director level position. Exceptionally well qualified candidates without prior pharmaceutical company experience may be considered.
· Prior clinical experience and strong academic track record in cardiovascular disease required.
· Experience in designing, monitoring and implementing clinical trials and interpreting trial results, including understanding of biostatistics, safety reporting, and regulatory requirements
· 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.
· Excellent presentation and interpersonal skills skills.
** Please note: Depending on experience, this role may be modified to that of the Associate Direrctor or Senior Director level.
|
| Johnson & Johnson Family of Companies |
|
PA |
11/19/2009
|
| Principal Research Scientist (Data Warehouse Administrator) - Radnor |
| A minimum of a PhD is required with at least 5 years of experience. Knowledge of biology and/or clinical science in the therapeutic areas of interest (immunology, oncology, etc.) is required. Must have excellent communication skills, demonstrated leadership skills, and the ability to operate in matrixed and global environment. Technical expertise with bioinformatics and/or medical informatics applications is required. Must have experience with database development in commercial setting as well as experience with data mining algorithms and applying them to biological and/or clinical problems. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Los Angeles |
CA |
11/19/2009
|
| Associate Director, Statistical Programming (Cougar Biotechnology) |
| BS degree in statistics, biostatistics, mathematics, computer science, or other relevant scientific areas is required; a MS or PhD degree in relevant areas is preferred. A minimum of 10 years of SAS programming experience with 5 or more years of clinical trials experience is required. This position requires 8-10 years of experience in the pharmaceutical/biotech industry. Ability to work with cross-functional teams a must. Good oral communication skills required. Prior experience managing a group is required. Prior work experience in the oncology area is preferred. Additionally, it is preferred that the candidate have excellent programming skills in SAS and/or S+ and other related tools; applied knowledge and understanding of clinical development programs and industry trends such as e-submission process and CDISC; and basic knowledge of software development life cycle, 21CFR Part 11, and other FDA regulations. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Millennium Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Clinical Research Manager II |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Medical Director |
|
| Millennium Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Sr. Manager, Clinical Operations |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Clinical Research Manager I |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Clinical Research Manager I |
|
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Medical Director |
| - Excellent oral and written communication skills.
- Working knowledge of biostatistics, clinical pharmacology and pharmacokinetics.
- Complete understanding of the drug development process.
- Keeps abreast of all regulatory updates and changes and disseminates information effectively and appropriately.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Medical Director, Cystic Fibrosis |
| ? MD, DO or equivalent ex-US medical degree
? 1-2 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 or a similar 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, 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 co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Scientist, Target Discovery -- Agensys, Santa Monica, CA |
| The successful candidate will have a PhD in molecular biology, biotechnology, biochemistry or related discipline with minimum 5 years of relevant industry experience. Other required experience includes expertise in a broad range of molecular and cellular techniques surrounding aspects of microarray-based discovery, biomarker identification and target selection for product development. Experience with management of research associates and demonstrated leadership is preferred. Excellent verbal and communication skills, as well as the ability to work in a dynamic team environment are essential. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Director/Senior Director, Molecular Discovery -- Agensys, Santa Monica, CA |
| ?X Advanced degree (Ph.D., or equivalent) with at least 10 years experience in an industry setting, molecular biology, molecular genomics, bioinformatics and related areas. with demonstrated track record of ?X Proven record in design and implementation of activities related to gene discovery and characterization, gene profiling, bioinformatics, ?X Demonstrated record in driving scientific and technical innovations, as evidenced by first or senior authored publications in top-tiered journals?X Demonstrated successful program leadership and multi-project coordination ?X At least 5 years of management experience of multiple groups ?X Proven track record in leading programs to achieve goals and timelines?X Ability to perform successfully in a cross-functional team environment?X Excellent written and verbal communication skills |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior Roles-Clinical Development & Medical Affairs, R&D |
| ? MD degree
? 10+ years experience in the Pharmaceutical industry in OTC and/or Rx Clinical research with commercial savvy
? Experience with development of overall clinical strategy and development plans
? Proven management experience at a senior level
? Demonstrates leadership behaviours by providing vision and direction
? Proven knowledge of drug development processes
? Be able to effectively liaise and influence internally and externally
? Excellent communication and interpersonal skills
? Fluency in written and spoken English, knowledge of French or other European languages beneficial but not essential |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Scientist, Pharmacokinetics |
| EDUCATION/EXPERIENCE:
Ph.D. with 1-3 years or MS with 5-8 years of experience in one or more areas biopharmaceutics, pharmacokinetics, drug metabolism, bioanalytical chemistry, biostatistics, PK modeling, in vivo-in vitro correlation (IVIVC), and clinical endpoint BE study design/conduct. Inhalation experience a plus. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Pharmacogenetic Analyst (CP) |
| 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 |
11/20/2009
|
| 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 |
MA |
11/20/2009
|
| Molecular/Cellular Biology Research Scientist (BS/MS) |
| B.S or M.S scientist with at least 3 years of relevant research experience; the candidate has strong background in cellular and molecular biology. Previous experience in the study of innate immunity is highly desirable; experience in cellular immunology and in vivo biology is advantageous. 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 thinking. Excellent communication and organization skills are required. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Head of Biostatistics |
| Ph.D. in Statistics or Biostatistics, plus 6-8 years of directly related managerial experience in In vitro diagnostics industry. Demonstrated management and leadership skills. Master the knowledge of statistical theory and applications pertaining to design of experiments, general linear models and variance components. Knowledge and experience in analysis of high dimensional data, especially clustering and classification methods and predictive statistical models for genetics and genomics data. Capable of technically addressing and solving unique statistical problems. Knowledge of appropriate regulatory agency regulations and guidelines. Excellent oral and written communication skills. Strong interpersonal and leadership skills. Ability to provide clear, technically sound, well-communicated guidance to non-statisticians. Self-motivated; ability to work independently and complete work on a timely basis. Skilled SAS programming knowledge; other statistical package knowledge a plus. Pharmaceutical/Biotechnology industry experience in assay validation, quality control, process optimization and validation, design of experiments, and pharmacokinetics. Experience with coordinating/tracking of resources, others? workloads and multiple projects. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Head of Bioinformatics & Biostatistics |
| Education:
Minimum ? MS, Desirable - PhD
Experience: Minimum - 8 years , Desirable ? 10 years.
Management experience: Minimum ? 4 years, Desirable ? 6 years. In vitro diagnostics experience essential.
Specific Professional Competencies:
- Must have proven proficiency in common statistical and data mining techniques used in analyzing biological data.
- Must have experience using R, Matlab, Spotfire, Partek or similar data analysis software.
- Proficiency in developing applications in high-level (Java, C++, C#) and scripting (Perl, Python, Ruby) programming languages to accomplish bioinformatics tasks. Familiarity with web frameworks such as Rails or Django is highly desirable.
- Experience using relational databases such as SQL Server, Oracle or PostgreSQL
- Knowledge of bioinformatics tools and databases such as the NCBI and UCSC Genome Browser, BLAST, Primer3, GEO and BioConductor
- Knowledge of pathway analysis and tools such as Ingenuity Pathway Analysis and GeneGo?s MetaCore is highly desirable.
- Familiarity with assay development and common laboratory techniques is highly desirable.
- Good understanding of molecular biology and diagnostic development is highly desirable.
- Must have excellent communication and presentation skills. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Fellow/Senior Fellow Safety Genomics |
| Education: MD, DVM or PhD in life sciences.
Extensive operational knowledge of histology and basic pathology.
Basic knowledge of molecular biology techniques and biomedical statistics
Experience: Significant scientific experience working in histology, pathology or molecular pathology
Technical Ability: Experience interpretation of gene expression profiles and integration in the context of a specific apthology/disease
Excellence in data summarization
Presentation: Excellent oral and written communication skills. Able to present and defend data and to influence the decision process regarding study design. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Computational Chemistry/Biology Research Investigator (Ph.D) |
| The ideal candidate will possess the following qualifications:
? Ph.D. degree in computational chemistry, computational biology or a related field, with 3+ years of related work experience.
? Familiarity with up-to-date biological screening paradigms.
? A proven track record in leveraging in silico techniques to drive basic science projects or in impacting hit finding activities in a drug discovery environment.
? A solid understanding of chemometrics, which includes QSAR methodologies, data mining and visualization, protein modeling, molecular docking, library design, conformational analysis, pharmacophore development, 2D and 3D similarity.
? A good understanding of bioinformatics and computational biology including gene expression data analysis and mining biological pathways to enhance target knowledge (GeneGO, Ingenuity).
? Demonstrate the ability to work independently as effectively as being able to collaborate in multidisciplinary teams.
? Strong analytical and problem-solving skills and scientific creativity are essential.
? Excellent oral and written communication skills and organizational skills are required.
The following qualifications are a plus:
? A solid experience in a pharmaceutical or biotech environment.
? Background in medicinal chemistry and basic knowledge of synthetic organic chemistry.
? Programming skills in C/C++/C#, Java and scripting in Perl/Python and Pipeline Pilot. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Bioinformatics, BMD Expert |
| Minimum requirements 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 candidate should 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, as is experience in a Unix/Linux environment. Familiarity with software packages such as Partek, GeneSpring, GeneData Analyst, and Matlab is also required. Experience with relational databases and SQL is a plus. 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.
Required years of experience One - Three Years
Education Doctorate Degree |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Bioinformatics - Oncology Translational Science |
| The ideal candidate will have an MS or higher in computational biology or a related field, with a minimum of 3-5 years research experience. A strong understanding of the application of statistics to biological problems, and experience in the analysis of genomic data, are required. Strong communication skills and a proven track record of interacting with scientific teams are also required. The candidate should be a strong scientific programmer, and ideally will be proficient in Perl and the R statistical language. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Associate Director, Patient Reported Outcomes(PRO) |
| ? Undergraduate degree in a relevant scientific/clinical discipline plus graduate degree (Masters or PhD) in relevant discipline including psychology, health economics, epidemiology, health services research, biostatistics, or public health.
? Minimum of 5 years of direct experience conducting PRO related research for pharmaceutical products.
? Demonstrated leadership experience and accomplishment and/or skill set necessary to manage in a cross functional team environment.
? Prior history of responsibility for development and execution of PRO strategy of products; experience managing products in all phases of development.
? Expert level knowledge in PRO analytical methods; thorough understanding of study designs that provide most relevant evidence to decision-makers; good knowledge of the regulatory and reimbursement environment.
? Familiarity with the regulatory guidelines and established best practices relating to PROs.
? Demonstrated research accomplishments including publications and presentations at scientific conferences.
? Good understanding/awareness of sources of clinical information including disease epidemiology and treatment.
? Thorough understanding of organizational processes, including significant experience working cross-functionally with Clinical Research, Marketing, Pricing, Market Access, and other functional areas.
? Established relationships with PRO thought-leaders. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Asc Director Biostatistics |
| Education (minimum/desirable):
PhD or Masters Degree (or equivalent degree) in Statistics, Data mining, Bioinformatics or related field with 3 years or 5 years of experience respectively for senior role.
Languages: Fluent English (oral and written).
Experience/Professional requirement:
? Proven knowledge and expertise in statistics, data mining and/or bioinformatics and their applications to clinical trials. Experience with a wide range of advanced statistical methods. Strong analytical capabilities and data exploration skills.
? Experience in main tasks of a program statistician and as a team leader.
? Proven knowledge of drug development.
? Background knowledge and strong interest in life sciences.
? Proven knowledge of general statistical software packages (e.g. SAS, R/Splus/MATLAB). Knowledge of specialized statistical/data mining tools.
? Good communication, presentation and consultancy skills.
? Creative mind with good problem solving skills. |
| Agilent Technologies, Inc. US |
AnaheimEl SegundoFolsomGarden GroveLa JollaMenlo ParkPalo AltoPleasantonRedwood CityRohnert ParkRosevilleSan DiegoSan FranciscoSan JoseSanta BarbaraSanta ClaraSanta RosaWestlake Village |
CA |
11/20/2009
|
| Product Marketing Engineer |
| ? Bachelor of Science in biology, biochemistry, molecular biology, bioinformatics, or related discipline required. Master or PhD preferred.
? Understanding of software tools used in copy number and SNP studies
? Ability to communicate and discuss technical information on copy number and SNP analysis/bioinformatics, genetics, and genomic studies.
? Knowledge of key software platforms for genetic analysis and bioinformatics tools and databases such as the eArray, DGV, NCBI and UCSC Genome Browser.
? Exceptional cross-functional communication skills - proven ability to influence at all levels of the organization.
? 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.
cb~10/01/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| Product Marketing Engineer |
| ? Bachelor of Science in biology, biochemistry, molecular biology, bioinformatics, or related discipline is required. Master or PhD preferred.
? Ability to communicate and discuss technical information on copy number and SNP analysis/bioinformatics, genetics, and genomic studies.
? Knowledge of key software platforms for genetic analysis and bioinformatics tools and databases such as the eArray, DGV, NCBI and UCSC Genome Browser.
? Exceptional cross-functional communication skills - proven ability to influence at all levels of the organization.
? 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. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| Applications Scientist - Microarrays & QPCR |
| Key Areas of Expertise:
Must have expertise in the following key areas:
-Microarrays ? Agilent arrays: Gene Expression, ChIP-on Chip, CGH
-QPCR ? both probe and SYBR Green assay experience desired
-Agilent Bioanalyzer
-Use of bioinformatics software, such as GeneSpring or ArrayAssist to analyze microarray data
Education/Experience:
?Must have a B.S. or M.S. in Biology, Molecular Biology, or Biochemistry. A PhD is preferred.
?5 years lab experience with microarrays and QPCR
?Lab experience with Stratagene and Agilent products is a plus
?Must be a team player
?Excellent verbal and written communication, organizational, and project management skills
-Ability to interface with global multidiscipline internal/external cross function teams
-Ability to demonstrate excellent outbound phone calling communication skills.
-Ability to solve a broad range of problems of varying scope and complexity.
-Proactively acts to understand customer needs and identify solutions to non-standard tasks/queries; actively creates business opportunities.
Geo Location: May reside in the Santa Clara, CA - La Jolla, CA - or Wilmington De Office
No relocation assistance available.
cb~10/08/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| 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:
? 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)
~cb~10/19/09 |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
11/20/2009
|
| Scientist II - Molecular Biology |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Senior Clinical Research Associate (IVD strongly preferred) |
| See above |
| openQ |
Charlottesville |
VA |
11/19/2009
|
| Data Research Project Manager |
| Skills:
Very thorough understanding of life sciences industry
Understanding of, and comfort with, reading medical literature and performing information searches on medically-related topics
Excellent verbal and written communication skills
Strong analytical skills and technical understanding of data acquisition, data structuring and data quality control
Prior experience interfacing with customers about data-related projects
Strong team player and the proven ability to work independently
Education:
PhD in life sciences field preferred or Masters degree and preferably at least 5 years relevant experience in life sciences driven data company
|
