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Field
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IRB submissions, amendments, consent forms, and continuing review materials Coordinate with UW offices (e.g., Human Subjects Review Committee, Grant and Contract Services, Environmental Health & Safety
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of visits and coordinates related facility and equipment availability. Reports and tracks adverse events (AE). Reports serious AEs to IRB and sponsor. Documents all protocol deviations, reconciles test
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— helping coordinate study timelines and deliverables, tracking budgets and milestones, supporting vendor and field-site relationships, and keeping research operations on schedule and in compliance with IRB
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informed-consent activities as permitted by the study protocol, IRB approval, institutional policy, and delegated study responsibilities. Review and follow study protocols, manuals of procedures, laboratory
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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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inconsistencies and monitors participant’s progress to include documentation and reporting of adverse events; resolves IRB/protocol management issues and recommends corrective action as appropriate; serves as
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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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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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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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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