- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... rigorous scientific and ethical standards.The Senior Director (Senior Principal Scientist ) has primary responsibility for the planning and directing clinical… more
- Sumitomo Pharma (Madison, WI)
- …a dynamic, highly motivated, and experienced individual for the position of Pharmacovigilance Scientist to perform PV activities for assigned programs(s). ... ongoing clinical trials. + Serve as a subject matter expert in Pharmacovigilance , including operations and medical, within the assigned program. + Support… more
- Takeda Pharmaceuticals (Boston, MA)
- …and empower you to shine? Join us as a PV Risk Management Scientist /Associate Director. At Takeda, we are transforming the pharmaceutical industry through our ... we do. As an Associate Director/ PV Risk Management Scientist , being part of our Risk Management and Benefit...Affairs, Biostats) to ensure alignment of global position for pharmacovigilance risk management processes to maximize patient safety +… more
- Lilly (Indianapolis, IN)
- …the practice of pharmacoepidemiology?** We are seeking an ambitious post-doctoral scientist with strong research and communication skills, to contribute to an ... from observational safety studies. In this role, the post-doctoral scientist will have the opportunity to + Develop a...and communicating high-quality safety information through the science of pharmacovigilance . The purpose of the GPS PE is to… more
- CVS Health (Blue Bell, PA)
- …and Aetna's Enterprise Data Warehouse (EDW). The Lead Decision Scientist role will have end-to-end responsibility of extraction-transformation-load including ... results, identify quality issues, investigate root cause, and assist Senior Decision Scientist , Senior Analyst, or Analyst in completing investigations as well as… more
- Lilly (Indianapolis, IN)
- …people around the world. The purpose of the Associate Director - Safety Data Scientist is to manage and analyze complex Global Patient Safety (GPS) datasets across ... trends, assess business issues, and drive analytic solutions. The Safety Data Scientist Associate Director / Director will work with stakeholders to analyze… more
- Merck (Rahway, NJ)
- **Job Description** Our Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... rigorous scientific and ethical standards. The Senior Director (Senior Principal Scientist ) has primary responsibility for the planning and directing clinical… more
- Boehringer Ingelheim (Ridgefield, CT)
- …& Clinical Pharmacology, CMC, Regulatory Affairs, Patient Safety and Pharmacovigilance to implement discovery and development toxicology strategies that enable ... the progression of optimized drug candidates. + When appropriate, take lead to develop plan and lead sub-team for investigative studies to support investigations on mechanisms of toxicity. + Serve as NDS Therapeutic Area lead, and/or provide guidance and… more
- Lilly (Indianapolis, IN)
- …and in support of the European Union Qualified Person for Pharmacovigilance (EU QPPV). **Benefit-Risk Management** **Leadership** **1) End-to-End Business Process ... internal expert to provide specialized knowledge within the area of Pharmacovigilance risk management and risk minimization activities. + Collaborate with… more
- BeOne Medicines (Emeryville, CA)
- …clinical development, program leadership, biometrics, clinical operations, safety/ pharmacovigilance , regulatory, molecular diagnostics, and translational research. ... at least one study through from start to finish in a clinical scientist role + Clinical oncology experience; candidates with exceptional experience in other… more
- BeOne Medicines (Emeryville, CA)
- …clinical development, program leadership, biometrics, clinical operations, safety/ pharmacovigilance , regulatory, molecular diagnostics, and translational research. ... at least one study through from start to finish in a clinical scientist role. + Clinical oncology experience; candidates with exceptional experience in other… 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 ... compounds. + Reviews and assesses overall safety information in conjunction with Pharmacovigilance and Medical Monitor of record for assigned compounds. + Oversees… more
- Taiho Oncology (Pleasanton, CA)
- …the development program. + Perform data review supported by Clinical Research Scientist (s) (CRS), participate in protocol deviation meeting that will occur monthly ... cross-functional areas (eg, clinical operations, biostatistics, data management, biomarker, pharmacovigilance , quality, etc.) + Knowledge in authoring key clinical… more
