- Bayer (St. Louis, MO)
- …routine and submission PV activities) and compliance with health authority pharmacovigilance (PV) regulations around the globe through the effective and timely ... completion of PV assessment activities. This is a senior clinical scientist position with deep expertise in key topics in pharmacovigilance (eg drug-induced… more
- Lilly (Indianapolis, IN)
- …for people around the world. **Purpose:** The Case Management Medical Review Scientist is responsible for conducting comprehensive medical review of Individual Case ... and responsibility of the European Union Qualified Person for Pharmacovigilance (QPPV). + Ensure support is provided to enable...or as work evolves. A Case Management Medical Review Scientist is expected to meet the criteria as outlined… more
- Sanofi Group (Morristown, NJ)
- …with colleagues from a number of different disciplines and development scientist is responsible for leading or representing clinical development across specific ... Data Managers, Global and Regional Study Managers, Feasibility Managers, Pharmacovigilance representative, Medical Writer (eg planning and review of narratives)… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …plan, working closely with Disease Area Head, Clinical Development Lead, Clinical Scientist . and other functional areas such as GCO, biostats, regulatory, ... pharmacovigilance . The Director will be a key contributor to INDs, NDAs, BLAs, and other global regulatory filings and publications. The Director will foster… more
- Takeda Pharmaceuticals (Boston, MA)
- …Development Team but more likely will oversee the study physician and/or clinical scientist leads responsible for leading the team. Emphasis will be on insuring that ... + Reviews and assesses overall safety information in conjunction with Pharmacovigilance and Medical Monitor of record for assigned compounds. + **External… more
- Lilly (Indianapolis, IN)
- …postdoctoral scientists and other researchers We are seeking an ambitious post-doctoral scientist with strong research and communication skills to contribute to the ... government, and academia. The candidate will develop key skills in pharmacovigilance and safety science (particularly with respect to novel methodologies), have… more
- Takeda Pharmaceuticals (Boston, MA)
- …may lead the US/EU Development Team but more likely will oversee the clinical scientist responsible for leading this team. Emphasis will be on insuring that the ... overall safety information for studies and compounds in conjunction with Pharmacovigilance . + **External Interactions** + Directs activities involved in interactions… more