- BeOne Medicines (Emeryville, CA)
- …field or biological science and 8+ years of experience as a Safety ( Pharmacovigilance ) Scientist . + MD (or internationally recognized equivalent) plus accredited ... **General Description:** The Director, Safety Scientist supports assigned compounds in conjunction with Product Safety Leads (PSLs) and leverages clinical and… more
- Merck & Co. (North Wales, PA)
- 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
- Merck & Co. (North Wales, PA)
- Job DescriptionOur Clinical Research and Pharmacovigilance team pushes the boundaries of global healthcare through research and innovation. Through clinical trials ... and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine.The Clinical Director is responsible for protocol development and medical/ scientific oversight of clinical research… more
- Arvinas (New Haven, CT)
- …more information, please visit www.arvinas.com . **Position Summary** The Clinical Scientist is responsible for providing scientific support for all Global Clinical ... medical experts both internal and external to the company. The Clinical Scientist needs to possess the ability to think creatively, function independently, deliver… 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
- Sumitomo Pharma (Providence, RI)
- …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
- 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
- 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
- Lilly (Indianapolis, IN)
- …+ Understand the roles and responsibilities of the EU Qualified Person for Pharmacovigilance (EU QPPV), if applicable. + Serve as an IT systems business quality ... + 2+ years experience in a quality control/quality assurance role supporting Pharmacovigilance (PV) + Experience in defined functional business areas, for example,… more
- Merck (Boston, MA)
- **Job Description** Our Clinical Research and Pharmacovigilance team pushes the boundaries of global healthcare through research and innovation. Through clinical ... trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine. The Clinical Director is responsible for protocol development and medical/ scientific oversight of 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
- Bayer (Whippany, NJ)
- …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
- J&J Family of Companies (Raritan, NJ)
- …the strategic direction of the Medical Safety Officers (MSO) and Safety Analysis Scientist TA Lead (SAS TAL) within Cardiopulmonary (CP) Therapeutic Area in Global ... Officer (CSO), the Chief Medical Officer (CMO) J&J IM, the Qualified Person for Pharmacovigilance (QPPV) and other J&J IM R&D leaders and the other groups within GMS… more
- Takeda Pharmaceuticals (Boston, MA)
- …Assesses overall safety information for studies and compound in conjunction with Pharmacovigilance . Oversees team with respect to assessment of these issues. + Makes ... + Interacts directly with research division, early clinical and clinical scientist , based on pertinent clinical and development expertise to provide knowledge… more
- Boehringer Ingelheim (Athens, GA)
- …and mitigations to resolve the issues. + Collaborates with the Clinical Scientist and Study/Trial team in protocol development, CRF design, writing amendments, ... (AE) reporting and request primary and follow-up information. + Provides information to pharmacovigilance and RA according to the study protocol and SOPs. + Ensures… 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
- 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
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