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University of North Carolina at Chapel Hill | Chapel Hill, North Carolina | United States | 14 days ago
of the trial will be implemented at UNC. Collaborating with institutional partners (investigators, IRBs, CTRC, and IDS) to complete all tasks required for site activation (writing and submitting IRB applications
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notes, and participant logs to help ensure safety. 7. Report and track adverse events (AEs). Reports serious AEs to PI, IRB and sponsor. 8. Review and manage clinical research study databases. 9. Educate
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report forms (CRFs) for accuracy, with guidance as needed. Maintains documents as required by FDA guidelines. May maintain contact with IRB and prepare and submit IRB documents. May ensure proper
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Posting Details Posting Details Job Title IRB Specialist Requisition Number RE55209 Working Title Department Name 40148:Office of Research Integrity Work Location Lexington, KY Grade Level 44 Salary
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5Geofield Contact City Bellinzona Website http://www.irb.usi.ch Street Via Chiesa, 5 Postal Code 6500 E-Mail [email protected] STATUS: EXPIRED X (formerly Twitter) Facebook LinkedIn Whatsapp More share
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investigator-initiated, including obtaining and submitting budget/billing information, implementing the IRB-approved recruitment plan, interacting with research participants, scheduling study visits, gathering
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University of North Carolina at Chapel Hill | Chapel Hill, North Carolina | United States | about 18 hours ago
deliverables. * Support IRB submissions, amendments, renewals, and regulatory documentation. * Coordinate participant recruitment, scheduling, data collection, and study activities as applicable. * Support
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research requirements and protocols. Specimen Collection (technicians rotate across these areas as needed) Clinic/pre-operative area: Gather IRB-approved clinical information (e.g., questionnaires) and
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contribute to IRB submissions; prepare research instruments; conduct community engaged research; collect, code and analyze quantitative and qualitative data; co-author and format fact sheets, briefs and/or
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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 article accountability