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Drug Safety Scientist Jobs

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This position is responsible for receiving safety related information via telephone calls, faxes, e-mails, etc., from Sponsors, CROs, healthcare professionals, study coordinators, allied health personnel, patients, caregivers and other parties reporting potential adverse events; entering data into safety database; preparing draft MedWatch and CIOMS I forms; following up on all SAE reports within r...

TechData is looking for Biostatistician, SAS Programmer, Outcome Research (HEOR), Contractor of Competitive Intelligence (BI), Contract Recruiter, Validation Leader/Pharmacovigilance Leader, Clinical Study Manager, Global Trial Leader, Clinical Data Manager, IMP Release Manager(Documentum EDI systems (TEDI,CREDI,REDI)), Information Specialist, Clinical Research Scientist, Safety Scientist/Drug Saf...

Job Description Qualified candidate will be hired at the appropriate level commensurate with education/experience. Description: This senior laboratory position supports R&D projects to improve safety assessments during discovery, development and clinical development phases with a specific focus on immunology and immunotoxicology. The incumbent develops and communicates immunotoxicology strategy...

Clinical/Regulatory - Safety Review Specialist Cambridge, MA DESCRIPTION • Responsible for aggregate review and reporting of safety data from various sources in support of regulatory aggregate reporting requirements, as well as safety surveillance and risk management activities. • This includes: o Creation, coordination, preparation, and completion of aggregate safety reports (e.g.PSUR, PBRER...

POSITION SUMMARY: The PV Scientist assists and supports the medical and scientific functions within safety evaluations for assigned products in clinical development and post marketing. Such tasks include preparation and coordination of reviews of individual case safety reports as well as aggregate safety data, including but not limited to, adverse effects and laboratory data. ESSENTIAL FUNCTIONS...

POSITION SUMMARY: The PV Scientist assists and supports the medical and scientific functions within safety evaluations for assigned products. Such tasks include preparation and coordination of reviews of individual case safety reports as well as aggregate safety data ESSENTIAL FUNCTIONS: The PV Scientist will also support Risk Management Plans by serving as a coordinator for the acquisition and...

The Drug Safety Scientist assists and supports the ongoing aggregate review and analysis of product safety for both pre and post-marketing data. Tasks include preparation and authoring of aggregate safety data including signaling analysis, DSUR, PSURs (Periodic Safety Update Reports), Annual Safety Reports, and reports to support internal/external data safety monitoring boards. The Drug Safety Sci...

Clinical/Regulatory - Safety Review Specialist Cambridge, MA DESCRIPTION •Responsible for aggregate review and reporting of safety data from various sources in support of regulatory aggregate reporting requirements, as well as safety surveillance and risk management activities.•This includes:oCreation, coordination, preparation, and completion of aggregate safety reports (e.g.PSUR, PBRER, PADER...

EMD Serono is the biopharmaceutical division of Merck KGaA, Darmstadt, Germany, a global pharmaceutical and chemical group. We strive to create value and benefit patients by transforming medical science into breakthrough solutions in our core therapeutic areas of neurodegenerative diseases, fertility and metabolic endocrinology, as well as oncology and autoimmune/inflammatory diseases as emerging ...

The Sr. Scientist in the PVRM Safety Information Management group is responsible for creating internal safety surveillance documents as well as safety reports for regulatory authorities for the company products, handling internal ad hoc queries/reports, analyzing/summarizing complex safety data, managing the operations of Safety Management Team (SaMT) meetings, managing signal detection activities...

The Sr. Scientist in the PVRM Safety Information Management group is responsible for creating internal safety surveillance documents as well as safety reports for regulatory authorities for the company products, handling internal ad hoc queries/reports, analyzing/summarizing complex safety data, managing the operations of Safety Management Team (SaMT) meetings, managing signal detection activities...

Advance your career with the company that makes it easier for people to choose better health. Express Scripts is a leading healthcare company serving tens of millions of consumers. We are looking for individuals who are passionate, creative and committed to creating systems and service solutions that promote better health outcomes. Join the company that Fortune magazine ranked as one of the "Most...

Job Description Qualified candidate will be hired at the appropriate level commensurate with education/experience. Description: This position is responsible for serving as the lead cross-functional interface to R&D projects and teams for managing discovery and investigative toxicology support. Lead and collaborate effectively with investigative and regulatory toxicology scientists to develop de...

Schedule: Full-time Job ID: 150003TZ Specific Job Duties : Safety Database administration Actively participate in the management of the installation, validation and configuration of Safety Database Responsible for the generation of Metric, Trending and Regulatory Reports Assist in the reconciliation process for safety programs Support the Safety Managers, Data Associates and Safety Scientist...

Description 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 g...

Postdoctoral Fellow - ADC(Anti-body drug conjugate) InVitro Safety Platform-15000003FE AbbVie (NYSE:ABBV) is a global, research-based biopharmaceutical company formed in 2013 following separation from Abbott Laboratories.The company's mission is to use its expertise, dedicated people and unique approach to innovation to develop and market advanced therapies that address some of the world's most c...

2015 will be the launch year of the AbbVie Post-doctoral Program. We are looking for the incoming class of Post Doc’s to join AbbVie as the company is positioning itself for another year of significant growth and advancement of patient-driven science and strategic therapeutic priorities. We have an exceptional Postdoctoral opportunity in our Investigative Toxicology and Pathology Group reporting t...

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...

PHARMACOVIGILANCE SAFETY SCIENTIST REQUIREMENT #15-01188 RECRUITER: CINDI PISNOY JOB LOCATION: HOPEWELL, NJ AUGUST 20, 2015 *** PharmD is a plus *** Project Description: Support Medical Safety Assessment Physicians (MSAP) in leading individual cross-functional Medical Surveillance Teams (MSTs) and assigned sub-teams, such as Safety Data Review (SDR) teams. Appropriately elevate program or p...

The statements made in this job description are intended to describe the general nature and level of work being performed by those persons assigned to this position. These statements are not intended to be an exhaustive list of all responsibilities, duties and skills required of people, nor will they necessarily all apply for every individual assigned to this position. DescriptionProvides advance...