• Associate Medical Director , Cardiology

    IQVIA (Durham, NC)
    …Minimum of 5 years' experience in clinical medicine, in addition to 4 years' clinical trials experience as an investigator or in the Pharma, CRO, or Biotech ... **Job Overview** The Associate Medical Director will provide medical, clinical and...school with a curriculum relevant to general medical education, clinical trials experience as an investigator or… more
    IQVIA (09/25/25)
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  • Clinical Contracts & Outsourcing Manager

    Kelly Services (South San Francisco, CA)
    …and ensuring compliance. The ideal candidate possesses a strong understanding of clinical trial processes, vendor functions, and financial oversight, coupled ... relationships. This role is critical in ensuring the successful execution of clinical trials through strategic outsourcing and effective vendor management.… more
    Kelly Services (10/03/25)
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  • Director , Program Operations Leader…

    Regeneron Pharmaceuticals (Warren, NJ)
    …leadership and overall strategic management of one or more complex programs in Clinical Trial Management (CTM). This individual is responsible for clinical ... (SOPs) within assigned program(s). The Dir POL is a member of the Clinical Trial Management extended leadership team, and as such interacts with senior level… more
    Regeneron Pharmaceuticals (08/19/25)
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  • Associate Director -Principal Medical…

    Sanofi Group (Morristown, NJ)
    …progress. The Principal Medical Writer is a key member of the Medical Writing team, the Clinical Trial Team (CTT) and Project Team. This is a position for a ... to ensure that the clinical opinion, as defined by the Clinical Study Director and the Therapeutic Department Head, is presented accurately and concisely. +… more
    Sanofi Group (09/06/25)
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  • Principal Medical (Science) Director , CVRM

    Genentech (South San Francisco, CA)
    …medical tactics by leveraging relevant expertise and insights. + Execute US Medical/global clinical trial activities conducted as part of Medical Affairs. **Who ... (CVRM) to join the Medical network at Genentech. The Principal Medical (Science) Director will provide exceptional clinical and scientific leadership for medical… more
    Genentech (09/06/25)
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  • Staff Clinical Compliance Auditor

    Danaher Corporation (Minneapolis, MN)
    …you will have the opportunity to: + Plan and execute internal audits of clinical trials , sites, vendors, and systems, and support external audits or regulatory ... of the Clinical Compliance team and report to the Sr. Director of Global Clinical Compliance responsible for clinical quality and scientific writing to… more
    Danaher Corporation (09/19/25)
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  • Director , Comparator Sourcing

    BeOne Medicines (Emeryville, CA)
    …Quality, CMC, Regulatory, etc.) stakeholders. + Demonstrates advanced knowledge of global clinical trials and the drug development process. + Experience in ... The Director of Comparator Purchasing, Clinical Supply Chain is responsible for overseeing the Clinical Supply Chain vision and strategy providing leadership… more
    BeOne Medicines (09/01/25)
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  • Senior Medical (Science) Director

    Genentech (South San Francisco, CA)
    …Position** **The Opportunity** The Sr. Medical Science Director / Sr. Medical Director will provide exceptional clinical and scientific leadership for medical ... clinically meaningful perspective for regulatory and other scientific communications + Clinical Study Design and Management + Scientific Engagement with Genentech's… more
    Genentech (10/02/25)
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  • Dermatology NPPA Clinical Specialist-…

    Bristol Myers Squibb (Atlanta, GA)
    …and unique perspectives in a supportive culture, promoting global participation in clinical trials , while our shared values of passion, innovation, urgency, ... have no direct reports and report into the Regional NPPA CS Director . The Dermatology Clinical Specialist will have materials created to support them in their… more
    Bristol Myers Squibb (08/30/25)
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  • Clinical Research Coordinator II - Center…

    Dana-Farber Cancer Institute (Boston, MA)
    …the Principal Investigator(s), the DFCI Clinical Trials Office, and the Clinical Research Director . The CRC II will be responsible for leading patient ... external auditing and study monitoring visits. + Coordination and management of clinical trials throughout the trial life cycle, including communication with… more
    Dana-Farber Cancer Institute (10/04/25)
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