• Associate Director , Search…

    AbbVie (San Francisco, CA)
    …to ensure an in-depth understanding of the science behind each of these opportunities. The Associate Director , Search & Evaluation will be a key member of the ... one aspect of Drug Development (eg, pre-clinical research, clinical development, Regulatory Affairs , Chemistry Manufacturing and Controls (CMC)). + Experience… more
    AbbVie (05/28/25)
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  • Director , GxP Auditing

    Gilead Sciences, Inc. (Oceanside, CA)
    …auditors, providing mentorship, performance evaluations, and long-term career development. The Director ensures compliance with global regulatory ... Define and execute a comprehensive audit strategy aligned with global regulatory expectations (FDA, EMA, MHRA, PMDA,...chains. + Certification in auditing (eg, ASQ, IRCA) or regulatory affairs . + Familiarity with digital audit… more
    Gilead Sciences, Inc. (08/14/25)
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  • Medical Director , Clinical Development…

    Ascendis Pharma (Palo Alto, CA)
    …clinical research resource for-cross-functional colleagues (eg in clinical operations, statistics, regulatory affairs , medical affairs , health economics ... Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe,...Those with less experience may be considered for an Associate Medical Director position. + At least… more
    Ascendis Pharma (07/04/25)
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  • Senior Medical Director , Late Development,…

    Pfizer (South San Francisco, CA)
    …design, conduct, and analysis. They work closely with other functions such as regulatory affairs , pharmacovigilance, biostatistics, and medical affairs to ... **Job Summary** The Senior Medical Director provides clinical development leadership and expertise for...the clinical development program meets the scientific, ethical, and regulatory standards. They also provides medical expertise and guidance… more
    Pfizer (08/21/25)
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  • Clinical Research Coordinator (CRC)

    General Dynamics Information Technology (Camp Pendleton, CA)
    …related to (TIME) clinical investigations.** **Communicates with research participants, staff, regulatory affairs and data management groups, laboratory and ... investigations as it relates to compliance with local, state, and/or federal regulatory requirements.** **Assists Principal / Associate Investigators in the… more
    General Dynamics Information Technology (08/14/25)
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