• Cancer Clinical Research Coordinator Associate…

    Stanford University (Stanford, CA)
    …case report forms for completion and accuracy with source documents. Prepare regulatory submissions , and ensure institutional Review Board renewals are ... + Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. + Determine eligibility… more
    Stanford University (08/30/25)
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  • CRA 2, Oncology, IQVIA Biotech

    IQVIA (San Francisco, CA)
    …to ensure compliance and data integrity. + Monitor study progress by tracking regulatory submissions , subject enrollment, case report form (CRF) completion, and ... and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. Your work will directly contribute to… more
    IQVIA (08/26/25)
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  • Executive Director of Biostatistics (Inflammation)

    Gilead Sciences, Inc. (Foster City, CA)
    …(TA), and oversee all biostatistics workstreams for clinical trials, assets evaluations, and regulatory submissions in the TA. The ideal candidate will have a ... programs. Partners and collaborates with cross-functional TA leads to meet the regulatory , scientific and business objectives. + Oversees and contributes to the… more
    Gilead Sciences, Inc. (08/23/25)
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  • Clinical Research Coordinator Associate (1 Year…

    Stanford University (Stanford, CA)
    …case report forms for completion and accuracy with source documents. Prepare regulatory submissions , and ensure institutional Review Board renewals are ... + Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. + Determine eligibility… more
    Stanford University (08/07/25)
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  • Clinical Research Coordinator Associate

    Stanford University (Stanford, CA)
    …audit study forms for completion and accuracy with source documents. Prepare regulatory submissions and ensure Institutional Review Board renewals are completed. ... activities. + Serve as primary contact with research participants, funders, and regulatory agencies. _* - Other duties may also be assigned_ **DESIRED… more
    Stanford University (08/07/25)
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  • Clinical Research Coordinator Associate

    Stanford University (Stanford, CA)
    …case report forms for completion and accuracy with source documents. Prepare regulatory submissions , and ensure institutional Review Board renewals are ... + Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. + Determine eligibility… more
    Stanford University (08/07/25)
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  • Medical Psychiatry Research Assistant(6 Month…

    Stanford University (Stanford, CA)
    …case report forms for completion and accuracy with source documents. Prepare regulatory submissions , and ensure institutional Review Board renewals are ... + Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. + Determine eligibility… more
    Stanford University (08/07/25)
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  • Clinical Research Coordinator Associate

    Stanford University (Stanford, CA)
    …case report forms for completion and accuracy with source documents. Prepare regulatory submissions , and ensure institutional Review Board renewals are ... *Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. *Determine eligibility… more
    Stanford University (08/07/25)
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  • Clinical Research Coordinator Associate

    Stanford University (Stanford, CA)
    …case report forms for completion and accuracy with source documents. Prepare regulatory submissions , and ensure institutional Review Board renewals are ... * Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. * Determine eligibility… more
    Stanford University (08/07/25)
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  • Associate Director, MSAT, Downstream Drug…

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    …and/or review technical reports, protocols, risk assessments, and relevant sections of regulatory submissions (IND, BLA, MAA, etc.) related to downstream ... processing. + Collaborate closely with Upstream MSAT, Validation MSAT, QA, Regulatory , Process Development, Analytical Development, and CDMO technical teams. + Stay… more
    Otsuka America Pharmaceutical Inc. (07/18/25)
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