- Merck & Co. (Boston, MA)
- Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... timely and equitable access to our medicines.The Senior Principal Scientist has primary responsibility for protocol development and medical/scientific oversight… more
- 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
- 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
- Parexel (Olympia, WA)
- …all Key Performance Indicators (KPIs) for the process + Function as pharmacovigilance representative/safety scientist + Attend/support Bid defense meetings + ... comprehensive medical reviews, provide expert safety monitoring, and deliver pharmacovigilance guidance across assigned projects. You'll also mentor junior team… more
- Merck (San Francisco, CA)
- **Job Description** Our Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... timely and equitable access to our medicines. The Senior Principal Scientist has primary responsibility for protocol development and medical/scientific oversight of… 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
- Astellas Pharma (Northbrook, IL)
- …interested in hybrid work are encouraged to apply. **Purpose:** The Development Scientist will participate in the development of clinical strategies for assigned ... Affairs, Clinical Operations, Data Sciences, Research, Translational Science and Pharmacovigilance (PV). + Demonstrated success working with key external… more
- Astellas Pharma (Northbrook, IL)
- …are encouraged to apply. **Purpose:** We are hiring an experienced real-world data scientist to join our Real-World Data Science (RWDS) team. As an Associate ... consumption and partner closely with Development, Medical Affairs, and Pharmacovigilance /Pharmacoepidemiology colleagues in their research. Additionally, you will collaborate… more
- J&J Family of Companies (Malvern, PA)
- …Johnson & Johnson Innovative Medicine R&D is recruiting for a Principal Scientist , Biopharmaceutics. This position is a hybrid role and will be located ... in Malvern, PA. We are seeking a highly motivated Principal Scientist to join the Biopharmaceutics team within the Drug Product Development and Delivery (DPD&D)… more
- Adecco US, Inc. (Clark, NJ)
- **Adecco Healthcare & Life Sciences is hiring a Scientist I, Post-Market Safety & Cosmetovigilance** for a **notable global cosmetics and personal-care company** ... **Pay:** **26- 29.4/hr** based on experience and education **Position Title:** ** Scientist I, Post Market Safety & Cosmetovigilance** **Location:** Clark, NJ… more
- J&J Family of Companies (Malvern, PA)
- …**We are searching for the best talent for a Principal Scientist , Lab Automation role to be in Malvern, PA.** **Purpose** : ... & Robotics team is recruiting for an Integrated Automation Principal Scientist to lead design, development, and implementation of end-to-end laboratory automation… more
- 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
- 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
- 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
