• Director, Clinical Operations

    Bausch + Lomb (Sacramento, CA)
    …evaluation, and selection of CROs and vendors (eg, central labs, central IRB , IVRS, etc.). + Manage the identification, evaluation, and selection of ... with the organization and management of DSMBs and Data Review Committees, as necessary. + Prepare study timelines and...to the IRBs/REBs/ECs. + Liaise with Data Management to review data discrepancies and ensure that data clarification forms… more
    Bausch + Lomb (06/07/25)
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  • Clinical Research Director

    UCLA Health (Los Angeles, CA)
    …to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH ... and human safety protection regulations and laws. + Demonstrated ability to interpret IRB , FDA, federal and UCLA requirements and utilize that information to guide… more
    UCLA Health (05/30/25)
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