• Senior Manager, Pharmacovigilance Scientist

    Bristol Myers Squibb (Princeton, NJ)
    …clinical trials, and project management skills; and + Medical concepts, safety activities in drug development, postmarketing, global safety health ... and three (3) years of post- baccalaureate experience. Must have experience with/in: + Drug safety , medical writing, signal detection, scientific background,… more
    Bristol Myers Squibb (05/07/25)
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  • Pharmacovigilance Reporting Analyst

    System One (Madison, NJ)
    …Life Sciences, Information, or similar background (Bachelors, Masters) + 5+ years Drug Safety / Pharmacovigilance experience + Advanced Tableau, Spotfire, ... Job Title: Pharmacovigilance Reporting Analyst Location: Lawrenceville, NJ Hours/Schedule: Hybrid...from the Source to Target + Support program and project team activities required to implement innovation initiatives. +… more
    System One (03/26/25)
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  • Associate Medical Director,…

    Sumitomo Pharma (Trenton, NJ)
    …English. **Education and Experience** + **Medical Degree (MD) with 3-5 years of drug safety experience in a pharmaceutical company** + Experience in oncology ... Mitigation Strategy (REMS) + Contributes to PVRM and cross-functional drug development teams and manages Safety Charters...+ Prepares and presents safety information (ie safety graphs, tables, and reports) to project more
    Sumitomo Pharma (05/16/25)
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  • Global Safety Officer, Oncology

    Sanofi Group (Morristown, NJ)
    … strategy and issue escalation with the Therapeutic Area Head (TAH) and Pharmacovigilance (PV) Head + Oversee third-party safety providers during acquisition and ... of medicine? The race is on to speed up drug discovery and development to find answers for patients...Communicate with and represent PV analyses and positions within project /productteams, in safety governance and benefit-risk governance… more
    Sanofi Group (05/24/25)
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  • Associate Director, Consumer Safety Science

    Haleon (Warren, NJ)
    …digital projects) within assigned therapeutic category and/or business unit and represent safety function at project teams and other relevant cross-functional ... with a risk-proportionate framework for product vigilance, the **Associate Director, Consumer Safety Science** is accountable for developing the safety strategy… more
    Haleon (05/17/25)
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  • Executive Director, Head of CoE, Global Medical…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …**Summary** The Executive Director, Head of Center of Excellence (CoE), Global Medical Safety will oversee a team of safety physicians and scientists across ... various regions, offering guidance and support to each product safety team in critical areas such as individual case...expectedness of the adverse event in relation to the drug . Ensure all relevant data and findings are incorporated… more
    Daiichi Sankyo Inc. (03/26/25)
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  • Director Clinical Development - Respiratory

    Teva Pharmaceuticals (Parsippany, NJ)
    …+ Resolves safety or relevant clinical issues in consultation with Global Drug Safety and Pharmacovigilance , SVP Late Clinical Development and the ... closely with other functional areas such as commercial, regulatory, pharmacovigilance , CMC, early clinical and pre-clinical development in this...+ Will be a core member of the Global Project Team + Will have and maintain the expertise… more
    Teva Pharmaceuticals (04/29/25)
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  • Associate Director, Laboratory Data Management

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …data in Daiichi Sankyo R&D collaborating with clinical and medical teams, clinical safety and pharmacovigilance , CROs and other vendors to ensure high quality ... possesses advanced knowledge of medical terminology capture and reporting of safety data, pharmacovigilance , industry best practices, and relevant regulatory… more
    Daiichi Sankyo Inc. (05/14/25)
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  • Associate Director, Data Management Processes,…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …of data in Daiichi Sankyo R&D collaborating with clinical and medical teams, clinical safety and pharmacovigilance , CROs and other vendors to ensure high quality ... of deliverables to support drug development processes and global submissions. This position provides...advanced knowledge of medical terminology capture and reporting of safety data, pharmacovigilance , industry best practices, and… more
    Daiichi Sankyo Inc. (04/22/25)
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  • Senior Clinical Research Director, Ophthalmology

    Sanofi Group (Morristown, NJ)
    …other medical and clinical scientific experts, clinical development scientists, in the project in collaboration with the Global safety Officer, Regulatory ... of medicine? The race is on to speed up drug discovery and development to find answers for patients...focused medical and scientific expertise to the cross functional project team to conduct the clinical studies from early… more
    Sanofi Group (04/22/25)
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