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minimum of 16.0 hours per week must be in-person at the IRB office on University of Utah campus. In-office requirements are subject to change per University and department policy. VP Area President
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serious AEs to IRB and sponsor. 6. Documents all protocol deviations, reconciles test article accountability at study close out and prepares summary report for sponsor. 7. Completes, audits, corrects CRFs
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Posting Details Posting Details Job Title Research Admin & Operations Director Requisition Number RE55690 Working Title Research Administration and Operations Director Department Name 7H854
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the direction of the PSTO/Adapt research manager to support the Principal Investigator’s research objectives. Depending on study needs, employees may have a hybrid work schedule after completing a probationary
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, medical history, and demographics, and maintain accurate documentation. Coordinate facility and equipment availability for study visits. Report adverse events, including serious AEs, to the IRB and sponsor
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Director will assist the IRB Director with all administrative activities associated with processing applications for IRB review. Principle Duties: Assist in the processing of all research applications
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Department: SOM KC Cardiovascular Medicine ----- CCR Admin Position Title: Clinical Research Manager - Cardiovascular and Cardiothoracic Research Job Family Group: Professional Staff Job Description
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notes, and 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
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physician-scientists, cares for 20,000 patients annually, and is home to more than 160 employees, plus all the physicians and clinical staff engaged in cancer patient care. The link to our website is: https
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by the convened IRB. Responsible for screening all clinical trial submissions for compliance with regulations governing the use of humans in research. Work with the Director and other UMCIRB staff