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forms, study advertisements, social media posts), and completing IRB applications. Train and coordinate research volunteers and research assistants to support projects. - 15% Manage launch activities
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logistics; IRB (both local and central) submissions and other applicable regulatory requirements; budgetary and contract review and approval. Provides direct patient care, including assessment, planning
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schedules with the study team. Reports and tracks adverse events (AE). Reports serious AEs to IRB and sponsor. Documents all protocol deviations, reconciles test article accountability at study close out and
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safety. 4. Determines length of visits and coordinates related facility and equipment availability. 5. Reports and tracks adverse events (AE). Reports serious AEs to IRB and sponsor. 6. Documents all
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interviews study subjects. Collects quantitative and qualitative data from subjects and/or medical records. Creates and manages documents for Institutional Review Board (IRB) and other study related activities
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-based research projects, helping to clarify concepts, research questions, and next steps. 4. Support faculty in preparing exempt IRB applications for classroom-based studies under supervision, ensuring
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sponsor progress reports. Assist in developing investigator-initiated, foundation, federal, and industry-sponsored research programs. Ensure compliance with institutional, IRB, IACUC, biosafety, sponsor
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the Institute for Health, Health Care Policy, and Aging Research (IFH), a unit of Rutgers Health. This position requires basic research skills (e.g,. literature reviews, IRB submissions, quantitative and
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approaches. Job Description Primary Duties & Responsibilities: Information on being a postdoc at WashU in St. Louis can be found at https://postdoc.wustl.edu/prospective-postdocs-2/ . Trains under
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with federal regulations, institutional policies, and sponsor requirements. This role serves as the primary regulatory liaison between investigators, the Institutional Review Board (IRB), study sponsors