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Arrangement - This position has the option to be 100% remote. Candidates must reside in one of the approved states for remote work, which can be viewed here: https://remotework.duke.edu/policy/outside-nc
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and monitor all processes. Study Regulatory Requirements (5%) Assure that all IRB and other pertinent UMN systems are adhered to including training requirements and record keeping. Assist in writing
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maintain IRB and regulatory approvals; conduct analysis, publish findings, and disseminate research findings through presentations at conferences and scientific meetings; (2) act as scientific liaison
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to determine resolution of AE. Reports serious AEs to IRB and sponsor. Presents related information to the community for recruitment purposes or to other research professionals in a variety of settings. Mentors
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to identify, evaluate, document, and report adverse events and safety concerns. Prepare and submit Institutional Review Board (IRB) applications, amendments, continuing reviews, and safety reports. Ensure
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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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Human Protections Specialist Requisition ID req37138 Working Title IRB Outreach Specialist Position Grade 13 Position Summary The University of New Mexico Health Sciences Center Human Research
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for assigned studies, preparing and overseeing IRB submissions (new applications, continuing reviews, amendments, reportable events, closures) and maintaining audit-ready regulatory files. • Coordinate
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IRB, GCP, and HIPAA (if applicable) guidelines Ensure adherence to protocol, IRB, GCP and HIPAA (if applicable) Ascertain that study staff are working within IRB, GCP, and HIPAA (if applicable
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, Clinical Research Center personnel, UNeHealth/SPA, accounting and IRB personnel to ensure optimal outcomes. Directs the research study team. Position Details Additional Information Posting Category