- Taiho Oncology (Princeton, NJ)
- …a dynamic, collaborative, and global cross-functional environment. Position Summary: The Director , Quality Assurance, ( Pharmacovigilance [PV]) reports into the ... PV and is responsible for partnering with the Sr. Director of QA, PV and PV colleagues to assure...Review and contribute to Safety Data Exchange Agreements (SDEA's), Pharmacovigilance Agreements (PVA's), or other Contracts to ensure GVP… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …Lead, Clinical Scientist. and other functional areas such as GCO, biostats, regulatory, pharmacovigilance . The Director will be a key contributor to INDs, NDAs, ... make a difference with. **The opportunity** The Clinical Trial Physician (CTP), Director , sits within Clinical Development and is responsible for contributing to the… more
- Taiho Oncology (Princeton, NJ)
- …an Associate Director in PV Sciences. At the forefront of pharmacovigilance innovation, we offer a dynamic and collaborative environment where your expertise and ... experience in our rapidly evolving organization. Position Summary: The Associate Director , PV Sciences role will lead medical surveillance activities for assigned… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **Position Overview** The Associate Director is responsible for ensuring that Primary Market Research, Competitive Intelligence, and Data ... Company policies and procedures, and governing body rules and standards. The Associate Director will: + Be a champion for ethical and compliant Primary Market… more
- Ascendis Pharma (Princeton, NJ)
- …a dynamic workplace for employees to grow and develop their skills. The Associate Director , ICSR Management Team reports to the Director , Head, ICSR Management ... + Raise or increase awareness, knowledge and understanding of pharmacovigilance requirements by conducting education/training sessions with functional partners /… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Development Scientific Director **Location:** Morristown, NJ Cambridge, MA **About the Job** Join the engine of Sanofi's mission - where deep ... that could turn the impossible into possible for millions. The Development Scientific Director (DSD) is a responsible member of the clinical team dedicated to the… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …training programs in GxP compliance, Ethics & Compliance, and Pharmacovigilance , ensuring alignment with regulatory requirements and business objectives. This ... (Good Manufacturing/Clinical/Laboratory Practice) compliance + Ethics and Compliance + Pharmacovigilance + Partner with Quality, Regulatory, R&D, Manufacturing, Supply… more
- Organon & Co. (Jersey City, NJ)
- …clinical development, late-clinical development, regulatory affairs, safety and pharmacovigilance , Chemistry, Manufacturing and Controls (CMC), medical affairs and ... for the general medicines portfolio of products. + Support Drug Safety and Pharmacovigilance with activities such as review of non-clinical literature for new risks,… more
- AbbVie (Jersey City, NJ)
- …as well as PMOS. PST lead will be interpreting regulations related to pharmacovigilance supporting all patient safety activities, and will be leading the safety ... products + Lead and set the strategy for key pharmacovigilance documents, including but not limited to, medical safety...DO, not required + 5 - 8 years of Pharmacovigilance (PST lead role equivalent) / Clinical Development experience… more
- Mallinckrodt Pharmaceuticals (Bridgewater, NJ)
- Job Title Senior Medical Director - Rheumatology Requisition JR000015351 Senior Medical Director - Rheumatology (Open) Location Bridgewater, NJ Additional ... Locations Job Description Summary The Senior Medical Director , Rheumatology, will serve as a critical member of the Global Medical Affairs team. They are responsible… more