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Field
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related field or equivalency (one year of education can be substituted for two years of related work experience). Some research experience. Knowledge of Good Clinical Practices, FDA, HIPPA, and IRB
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of research projects, including IRB submissions, participant recruitment, study visits, data collection, and timely submission of study data to sponsors. The ideal candidate will have a strong work-ethic
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and knowledge of Institutional Review Board (IRB) processes Demonstrable experience with using scripting/programming languages in task automation and/or data pipelines Ability to effectively utilize
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agencies, or specially designated review groups. Understand the IRB submission and review process and when and how to apply for IRB review, including facilitation of study initiation through meticulous and
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, quarterly, annual, and milestone-triggered); facilitating IRB protocols and human subjects research compliance; managing workshop and event logistics (venue, catering, participant travel, lodging, and
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University of North Carolina at Chapel Hill | Chapel Hill, North Carolina | United States | about 1 month ago
, analysis, and team collaboration. Knowledgeable about domestic and international institutional review board (IRB) policies and processes and able to maintain study documentation, protocol submissions, and
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offices. Assists with IRB submissions, amendments, continuing reviews, and other regulatory requirements. Ensures collection and maintenance of required investigator and study staff documentation, including
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external sponsors as needed, Manage IRB protocols and ensure ethical research compliance, Maintain research equipment (driving simulators, VR headsets, eyetracking glasses, motion capture inside out/outside
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staff. Maintains equipment and supply records and assists with purchasing and inventory tracking. Coordinates laboratory access, onboarding, and required training to support IRB compliance and processing
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clinicians across LCCC consortium sites. Institutional Departments and Staff: Institutional Review Board (IRB), Office of Research Quality Assurance (ORQA), Clinical Research Operations Office, MedStar Health