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. 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 for
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. 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 for
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. mail. Work with Academic Advising team to ensure smooth transfer from recruitment to matriculation. Actively track and report out on prospective student recruitment 3. Develops and communicates
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/biospecimens Report and track adverse events Document all protocol deviations, reconcile test article accountability at study close and prepare summary report for department and sponsor Attend team and study
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sharing. Collaborates with the Alumni Relations team to develop the logic and system for an alumni engagement score, creates a tracking system for alumni affinity groups, and oversees data integrity
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and clinical measurements from study participants (phlebotomy training will be provided as needed) Assist in packaging and shipping of samples/biospecimens Report and track adverse events Document all
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and clinical measurements from study participants (phlebotomy training will be provided as needed) Assist in packaging and shipping of samples/biospecimens Report and track adverse events Document all
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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 sponsor
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, overseeing study visits and acting as a liaison between participants and study-related parties. 4. Recognizes, tracks and reports adverse events and protocol deviations. 5. Prepares for and coordinates site
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subject log to help ensure subject safety. Determines length of visits and coordinates related facility and equipment availability. Reports and tracks adverse events (AE). Reports serious AEs to IRB and