• Daiichi Sankyo, Inc. (Bernards, NJ)
    …in PV; required10 or more years of experience within Drug Safety / Pharmacovigilance experience, including both investigational and marketed products; ... oversight groups for case processing activities and reports to the Director of PV Case Management.Responsibilities:ICSR Processing: Oversees QC activities, supports… more
    HireLifeScience (07/09/25)
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  • Associate Medical Director

    Sumitomo Pharma (Pierre, SD)
    …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Medical Director .** The Associate Medical Director ... for SMPA investigational and commercial products. The incumbent will provide medical safety support for safety signal management throughout product lifecycle… more
    Sumitomo Pharma (05/16/25)
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  • Associate Director , Safety

    BeOne Medicines (San Mateo, CA)
    **General Description:** _The Associate Director , Safety Scientist supports assigned compounds in conjunction with Product Safety Leads (PSLs) and ... in departmental activities **Supervisory Responsibilities:** This position has no direct reports. The Associate Director , Safety Scientist is part of a team… more
    BeOne Medicines (07/08/25)
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  • Associate Director , Clinical…

    Takeda Pharmaceuticals (Boston, MA)
    …true to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ... in partnership with functional compliance teams for regulations impacting Clinical, Safety and Clinical Pharmacovigilance Medical Quality (CPMQ) processes and… more
    Takeda Pharmaceuticals (04/25/25)
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  • Associate Director - Global Patient…

    Lilly (Indianapolis, IN)
    …around the world. **Purpose:** The purpose of the Global Periodic Aggregate Safety Reports Scientist is to ensure effective and accurate interpretation of global ... practices in the industry. **Primary Responsibilities** **1. Global Periodic Aggregate Safety Report Technical Expertise** + Ensure periodic report deliverables meet… more
    Lilly (07/02/25)
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  • Associate Director , Postmarketing…

    United Therapeutics (Phoenix, AZ)
    …You are passionate about PV and enjoy being part of a collaborative team. The Associate Global PV Case Management Director plays a key role in management and ... oversight of end-to-end case safety management activities spanning across our global commercial product...is critical in ensuring that commercial operational aspects of pharmacovigilance activities are managed with rigorous global standards in… more
    United Therapeutics (05/21/25)
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  • PV Risk Management Scientist/ Associate

    Takeda Pharmaceuticals (Boston, MA)
    …you and empower you to shine? Join us as a PV Risk Management Scientist/ Associate Director . At Takeda, we are transforming the pharmaceutical industry through ... strive for excellence in everything we do. As an Associate Director / PV Risk Management Scientist, being...Affairs, Biostats) to ensure alignment of global position for pharmacovigilance risk management processes to maximize patient safety more
    Takeda Pharmaceuticals (05/22/25)
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  • Temp - Associate Director

    System One (Tarrytown, NY)
    Job Title : Temp - Associate Director , Aggregate Reporting, GPS Type: Contract Compensation: $85 - $100 hourly (dependent on experience) Contractor Work Model: ... Remote Highlights should include: 1. Pharmacovigilance & Aggregate Reporting Expertise + Direct experience authoring...interpret clinical data to support benefit-risk assessments. Temp - Associate Director , Aggregate Reporting, GPS + Submit… more
    System One (06/24/25)
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  • Associate Director , Consumer…

    Haleon (Warren, NJ)
    …supplements. In line with a risk-proportionate framework for product vigilance, the ** Associate Director , Consumer Safety Science** is accountable for ... for medium to high-risk products. The position holder will: + Develop safety strategy for medium to high-risk products within the assigned therapeutic category… more
    Haleon (07/08/25)
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  • Compliance Operations Lead, Associate

    Takeda Pharmaceuticals (Boston, MA)
    …Lead CPMQ continuous improvement initiatives to enable optimization of clinical and safety quality compliance activities. + Provide expert advice and support to the ... CPMQ activities eg audit, inspection, QE, CAPA. + Organise Clinical and Pharmacovigilance Quality council meetings and proactively manage the agenda and ensure key… more
    Takeda Pharmaceuticals (07/12/25)
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  • Associate Medical Director

    Takeda Pharmaceuticals (Cambridge, MA)
    …company that will inspire you and empower you to shine? Join us as an Associate Medical Director in our Neuroscience Therapeutic Area Unit in our Cambridge, MA ... to our inspiring, bold mission ​ **​POSITION OBJECTIVES** : ​The Medical Director leads and drives strategy for the overall global clinical development of… more
    Takeda Pharmaceuticals (06/19/25)
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  • Medical Director , Oncology Early…

    AbbVie (South San Francisco, CA)
    …LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Medical Director leads the direction, planning, execution, and interpretation of clinical ... integrity, and review, interpretation, and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is… more
    AbbVie (05/14/25)
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  • AD/SR AD, US Product Group RA, US RRL - Cardio…

    Boehringer Ingelheim (Ridgefield, CT)
    …Specialized Pharmacist or Master of Drug Regulatory Affairs, RAC certification preferred ** Associate Director Experience Requirements:** + Two (2) years of ... professional experience in a scientific, clinical, and/or medical space. **Sr. Associate Director Requirements:** + Five (5) years of professional experience in… more
    Boehringer Ingelheim (05/09/25)
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