172 irb-director "https:" positions

  • Georgetown University | Washington, District of Columbia | United States | 22 days ago

    analyst will work under the direction of the Senior Director of the OHSP to manage the administrative functions necessary for the successful operations of the office.  These functions include being the

  • University of Utah | Salt Lake City, Utah | United States | about 21 hours ago

    maintain accurate documentation. Coordinate facility and equipment availability for study visits. Report adverse events, including serious AEs, to the IRB and sponsor. Document protocol deviations

  • University of North Carolina at Chapel Hill | North Wilkesboro, North Carolina | United States | 6 days ago

    oversight by this office resulted in harms to human subjects. The IRB Vice Chair reports to the Director of the Office of Human Research Ethics and through the Director to the Vice Chancellor for

  • University of Utah | Salt Lake City, Utah | United States | about 21 hours ago

    participant logs to help ensure safety. 7. Report and track adverse events (AEs). Reports serious AEs to PI, IRB and sponsor. 8. Review and manage clinical research study databases. 9. Educate staff regarding

  • Black Hills State University | Spearfish, South Dakota | United States | about 16 hours ago

    /contract compliance requirements Support Grant Director, IRB Chair and IRB Committee with minutes, record-keeping and reporting requirements. Support other grants office functions such as drafting

  • University of Washington | Seattle, Washington | United States | about 17 hours ago

    Job Description The Department of Ophthalmology has an outstanding opportunity for Research Coordinator 4 to join their team. OVERVIEW : Reporting to the Associate Director of Research, the Research

  • University of Utah | Salt Lake City, Utah | United States | about 21 hours ago

    accurate documentation. Coordinate facility and equipment availability for study visits. Report adverse events, including serious AEs, to the IRB and sponsor. Document protocol deviations, reconcile test

  • University of Utah | Salt Lake City, Utah | United States | about 21 hours ago

    tracks adverse events (AE). Reports serious AEs to IRB and sponsor. Documents all protocol deviations, reconciles test article accountability at study close out and prepares summary report for

  • University of Utah | Salt Lake City, Utah | United States | about 21 hours ago

    availability. Reports and tracks adverse events (AE). Reports serious AEs to IRB and sponsor. Documents all protocol deviations, reconciles test article accountability at study close out and prepares

  • University of Utah | Salt Lake City, Utah | United States | about 1 month ago

    . Reports and tracks adverse events (AE). Reports serious AEs to IRB and sponsor. Documents all protocol deviations, reconciles test article accountability at study close out and prepares summary report

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