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Field
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serious AEs to IRB and sponsor. 4. Presents related information to the community for recruitment purposes or to other research professionals in a variety of settings. 5. Mentors and trains new and
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, to the IRB and sponsor. Document protocol deviations, reconcile test article accountability, and prepare summary reports. Complete, audit, correct, and relay CRFs to the sponsor. Assist with negotiating
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protocols. Under supervision of MnDRIVE and Psychiatry Regulatory Specialist, creates regulatory files for new studies. Completes IRB and other required review committee applications on assigned protocols
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Center for Clinical and Translational Research (NeCCTR) and its associated units; working in close coordination with the VCR Director of Business Operations, VCR Director of Research Finance Operations and
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Manager for various and unanticipated worksites throughout the U.S. (HQ: Chicago, IL)." Coordinate and oversee execution of research projects. Manage the day-to-day activities and the overall workflow
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, including coordination, organization and maintenance of all documentation required by Sponsor or CRO as well as working with partnering institutions on managing invoicing, and IRB paperwork under limited
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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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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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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