• Sponsor Dedicated Regulatory

    IQVIA (Durham, NC)
    …(WIs), quality of designated deliverables and project timelines. * Perform start up and site activation activities according to applicable regulations, SOPs ... documents to sites and internal project team members. * Prepare site regulatory documents, reviewing for completeness and accuracy. * Ensure accurate completion and… more
    IQVIA (10/23/25)
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  • Clinical Research Associate - Sponsor

    IQVIA (Durham, NC)
    …required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions * Perform site monitoring visits (selection, ... and close-out visits) in accordance with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on… more
    IQVIA (10/18/25)
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  • (Senior) Clinical Research Associate…

    IQVIA (Durham, NC)
    …required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions * Perform site monitoring visits (selection, ... and close-out visits) in accordance with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on… more
    IQVIA (10/13/25)
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