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for IRB submissions and compliance. Contribute substantively to grant applications, progress reports, and manuscripts, including methods, analytic plans, preliminary data, and coordination of co
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for electronic and paper-based research records. Maintain compliance with HIPAA and IRB regulations and guidelines. Minimum Qualifications High school diploma or graduation equivalent. Six months of work
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, assisting in IRB submission activities, budget and billing, and ensuring overall compliance with all federal and local guidelines. Primary Duties and Responsibilities Works under the direction of a Clinical
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, improving efficiency, and training of personnel. The incumbent ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB
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., HIPAA, IRB, FDA). Project management certification or equivalent leadership training. About the Department The Center for Learning Health System Sciences is a one-of-a-kind partnership between the Medical
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-solving skills Ability to thrive in both team and independent work environments Strong organizational and communication skills Experience with human-subjects research protocols, IRB processes, or Good
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assistance with compliance, IACUC, IRB and FDA application coordination, liaison to all internal and external stakeholders, and preparation of sponsor reports. Conducts research and coordinates collaborations
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University of North Carolina at Chapel Hill | Chapel Hill, North Carolina | United States | about 1 month ago
proactively with minimal supervision. Preferred Qualifications, Competencies, and Experience * Experience with human subjects research projects * Familiarity with Institutional Review Board (IRB) processes and
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Posting Number req26704 Department Psychiatry Department Website Link https://psychiatry.arizona.edu/ Location Tucson Campus Address Tucson, AZ USA Position Highlights Dr. Killgore is seeking a Research
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over 150,000 inpatient discharges per year. All parts of YNHHS are interconnected within a single electronic medical record and a unified IRB, making it an ideal platform for clinical research at scale