Drug Safety Scientist Jobs

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61 Drug Safety Scientist jobs found on Monster.

Jobs 1 to 20 of 61
TechData is looking for Scientist I, Scientist II, Biostatistician (on site or telecommuting), SAS Programmer/Statistical Programmer/telecommuting, CDISC programmer (remote, multiple positions as sr. or lead positions), Java Programmer (Remote), Medical Writer, Sr. Clinical Data Manager, Drug Safety Specialist for our pharmaceutical clients in Central and Northern NJ. Please see below requirements...
Company: Yoh Senior Patient Safety Scientist needed for a contract opportunity with Yoh's client located in Gaithersburg, MD. The Big Picture - Top Skills You Should Possess: - Working with the Global Safety Physician (GSP), take responsibility for aspects of the Clinical Safety strategy for assigned drug projects and products throughout all stages of development and/or when on the market, includi...
Job Description: We are seeking a highly motivated Principal Scientist (Toxicologist or Pathologist) with experience in GLP toxicology, drug development, regulatory submissions, and leadership experience on nonclinical development teams to support developing innovative antibody and small molecule based therapies that improve outcomes for patients with cancer and autoimmune diseases. Responsibiliti...
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we l...
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we l...
BIOANALYTICAL SCIENTIST WITH HPLC EXPERIENCE REQUIREMENT #14-00666 RECRUITER: KAREN GULUTZ JOB LOCATION: DEVENS, MA JULY 7, 2014 * Shift: SUNDAY - WEDNESDAY, 2nd Shift 2pm-12:30 am * Project Description: Temporary Quality Control Analyst to support Rheumatoid Arthritis Drug while other analyst is dedicated to a Cancer Drug bioassay validation and spec setting GMP Assists in the development, valida...
SENIOR PHARMACOVIGILANCE SCIENTIST REQUIREMENT #14-00668 RECRUITER: MICHELLE ASHEN JOB LOCATION: GAITHERSBURG, MD JULY 7, 2014 * CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 * Project Description: Working with the Global Safety Physician (GSP), take responsibility for aspects of the Clinical Safety strategy for assigned the client’s MedImmune drug projects and products throughout all st...
The Colonial Group specializes in the placement of outstanding talent in FDA Regulated Manufacturing Environments and organizations that sell to those environments. Our clients understand that our decades of industry experience give us unique insight and access to top talent at all levels. The Colonial Group is a nationally recognized, award-winning firm dedicated to helping both clients and candi...
AMEC is a focused supplier of consultancy, engineering and project management services to its customers in the world's oil and gas, mining, clean energy, environment and infrastructure markets. With annual revenues of some £4.2 billion, AMEC designs, delivers and maintains strategic and complex assets and employs over 29,000 people in around 40 countries worldwide. See amec.com. AMEC shares are tr...
Company Overview: Lilly is the 10th largest pharmaceutical company in the world, and has been creating medicines that help improve peoples' quality of life for more than 135 years. Across the globe, we are a leader in investing in research and development and we also invest in our employees – in competitive salaries, training and development, and health. The pharmaceutical industry is a complex, r...
ASSOCIATE PHARMACOVIGILANCE SCIENTIST REQUIREMENT #14-00713 RECRUITER: CINDI PISNOY JOB LOCATION: GAITHERSBURG, MD JULY 16, 2014 * CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 * Project Description: Safety Governance and Risk Management activities Working with the Global Safety Physician (GSP), support the Clinical Safety strategy for assigned drug projects and products throughout all s...
PRINCIPAL PHARMACOVIGILANCE SCIENTIST REQUIREMENT #14-00712 RECRUITER: KAREN GULUTZ JOB LOCATION: GAITHERSBURG, MD JULY 16, 2014 * CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 * Project Description: Safety Governance and Risk Management activities Working with the Global Safety Physician (GSP), be responsible for the Clinical Safety strategy for assigned drug projects and products throu...
TechData is hiring SAS Programmer, Biostatistician, Clinical Data Manager, Clinical Research Scientist/Clinical Study Manager for our pharmaceutical clients in Northern NJ. Please see below requirements and send your resume to: *****. TechData is a leading provider for temporary and permanent positions in the pharmaceutical industry. TechData offers very competitive pay ra...
Company: Yoh Clinical Research Scientist needed for a contract opportunity with Yoh's client located in Summit, NJ. Top Skills Should You Possess: - Clinical operations - Oncology What You'll Be Doing: - Assist the Clinical Research Scientist team to interface with project team members including: Clinical Research Physician, Clinical Operations, Data Management, Statistics, Drug Safety, Regulatory...
Senior Scientist I sought by EMD Serono Research and Development Institute, Inc., developer of pharmaceutical products, to propose new targets, therapeutic concepts, or technological approaches to relevant Committees (i.e. decision-making bodies). Read and critically evaluate scientific literature relevant to Research strategy. Write relevant sections for Discovery Project Proposals (DPP), and coo...
Leading pharma client seeks a Senior Pharmacovigilance Scientist for a 6 month contract opportunity. The general responsibilities for the Senior Pharmacovigilance Scientist are the same as for the Pharmacovigilance Scientist, although it is expected that given greater knowledge and experience such responsibilities may be required for one or more products of high business priority and/or complexity...
Scientist – Developmental Toxicology Location: Cambridge, MA Akebia Therapeutics is looking for Toxicologist to work with an integrated individual group responsible for developing our understanding of the biological fate of candidate drug molecules from pre-clinical studies through clinical investigation., This person will provide the execution of the strategy for generating the Toxicology and ADM...
Senior Veterinary Scientist II - 70069028-37197 Description The individual must be a veterinarian who possesses a broad base of knowledge in the field of veterinary medicine and research. Ensures effective protocol design and conducts clinical and safety trials to evaluate developmental products. Ensures regulatory compliance by being completely cognizant of all Good Laboratory Practices and Good...
Position Summary Principal Scientist or Senior Scientist, Formulation Position Summary Responsible for the design and development of complex immediate and modified release parenteral formulations containing either small molecule or Peptide APIs. Primary focus will be on biodegradable peptide formulations: nanoparticles, liposomes and drug-polymer conjugates. Utilize Quality by Design (QbD) for for...
The laboratory groups at are responsible for the support of pharmaceutical product development in a range of dosage forms both directly with customers and in collaboration with other Catalent facilities. This includes formulation development, structural chemistry, analytical support and clinical trials material manufacturing. The Lead Scientist works with minimum supervision, conferring with super...
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