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Field
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(PI) guidance to meet the research objectives of the project. Assists with study start-up activities including IRB applications for initial review, modifications/amendments, continuing reviews, and
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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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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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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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study status reports and maintaining study documentation. Submission of protocol, consent documents for IRB approval and assist in preparing regulatory submissions as requested Work at UF research
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University of North Carolina at Chapel Hill | Chapel Hill, North Carolina | United States | about 16 hours ago
institutions. Management Preferences Experience initiating and updating IRB and PRC applications Experience in an oncology-related field Experience with Epic@UNC, RedCap, Access, or other Microsoft Office
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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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University of North Carolina at Chapel Hill | Chapel Hill, North Carolina | United States | about 16 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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Clinical Research Coordinator - Sarver Heart Center Posting Number req26826 Department Sarver Heart Center Department Website Link https://heart.arizona.edu Location Tucson Campus Address 1501 N. Campbell
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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