• Director R&D Quality - Intelligence…

    Gilead Sciences, Inc. (Parsippany, NJ)
    …drug development process and GxP requirements (ie, clinical studies, post-marketing/ pharmacovigilance , and labs). + Thorough knowledge of standards, systems, ... paid time off, and a benefits package. Benefits include company-sponsored medical , dental, vision, and life insurance plans*. For additional benefits information,… more
    Gilead Sciences, Inc. (05/06/25)
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  • Global Regulatory Director

    Edgewell Personal Care (Allendale, NJ)
    …for assessing, interpreting, and following global regulations for OTC drugs, medical devices, cosmetics, biocides and consumer goods. Ensures standards are ... + Experience with OTC drug regulations for FDA, Health Canada, and TGA. Medical devices's regulations in the USA, Canada, and Mexico. + Experience with global… more
    Edgewell Personal Care (03/04/25)
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  • Associate Director , Labeling

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... 3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core Data Sheets (CCDS)… more
    Daiichi Sankyo Inc. (05/09/25)
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  • Head of ICSR Management - Job ID:

    Ascendis Pharma (Palo Alto, CA)
    …mission of developing new and potentially best-in-class therapies to address unmet medical needs. Our culture fosters a place where skilled, adaptable, and highly ... Management Leads working on a diverse scope of activities to ensure pharmacovigilance regulations/ guidelines are adhered to. + Responsible for managerial oversight… more
    Ascendis Pharma (05/04/25)
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  • Veterinarian, Vet Technical Solutions

    Boehringer Ingelheim (Duluth, GA)
    …questions. All communications will be recorded in the BIAH Pharmacovigilance (PV)Database in compliance with BIAH corporate, Veterinary Technical Solutions ... and within the approved timeliness. + Stays current with medical and technical knowledge relevant to BIAH products. +...involving product usage. + Supports the AD, SAD or Director in projects as assigned. + Participates in the… more
    Boehringer Ingelheim (05/13/25)
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  • Global Category Manager - Clinical Development…

    Takeda Pharmaceuticals (Boston, MA)
    …Category Manager (GCM) - Clinical Development Services Procurement at the Associate Director level, plans and leads category projects for a clearly defined ... or buying of Compliance Services categories, including but not limited to pharmacovigilance services.** You will be assigned to support Takeda's Research &… more
    Takeda Pharmaceuticals (05/02/25)
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  • VP-Regional Medical Officer (Internal…

    ThermoFisher Scientific (Carlsbad, CA)
    …Office **Job Description** Summarized Purpose: Serves as the West Coast Regional Medical Officer for PPD Biotech . Focuses on business development and client ... Delivers strategic value to Biotech clients from an industry experienced medical and scientific leadership perspective. Deliverables are strongly aligned with West… more
    ThermoFisher Scientific (05/15/25)
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  • AD/SR AD, US Product Group RA, US RRL - Cardio…

    Boehringer Ingelheim (Ridgefield, CT)
    …the assigned therapeutic area from the regulatory, legislative, scientific, medical , pharmaceutical, pharmacovigilance , market access and commercial perspective. ... + Two (2) years of professional experience in a scientific, clinical, and/or medical space. **Sr. Associate Director Requirements:** + Five (5) years of… more
    Boehringer Ingelheim (05/09/25)
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  • Clinical Scientist II

    AbbVie (South San Francisco, CA)
    …Tok (https://www.tiktok.com/@abbvie) . Job Description In collaboration with a therapeutic area Medical Director or Scientific Director , the Clinical ... medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's… more
    AbbVie (05/09/25)
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  • Manager, Safety Analysis Scientist

    J&J Family of Companies (Horsham, PA)
    …and Skills:** **Required** + 6+ years of relevant experience is required. + Medical writing or Pharmacovigilance (PV) experience is required. + Working knowledge ... safety assessment of assigned products. In partnership with the Medical Safety Officer (MSO), the manager is responsible for...will function independently, or with moderate guidance from the Director , SAS Therapeutic Area Lead (TAL), be able to… more
    J&J Family of Companies (05/24/25)
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