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of operations and training materials; preparing, submitting, and maintaining IRB documentation; coordinating with domestic and international collaborators; and ensuring high protocol fidelity across study sites
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Coordinator II. The Clinical Research Regulatory Coordinator II will prepare, submit, and assist with multiple levels of research documentation, IRB submissions to UAB, WIRB, Advarra, and others. Maintain
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Employee Class Acad Prof and Admin Add to My Favorite Jobs Email this Job About the Job Position Summary The Assistant Director of Research – Clinical Manager provides clinical and operational leadership
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benefits, a wide variety of professional development opportunities, supportive work and family benefits, a wealth of health and wellness programs and resources, and much more. Posted Job Title Manager
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-to-date knowledge of human subject research protections and IRB regulations. Works with researchers, the IRB Chairperson(s) and members, the Human Research Compliance Director, IRB staff and other
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Human Brain Imaging Research (CAHBIR; (https://sites.rutgers.edu/cahbir/ ). We seek candidates with expertise in network neuroscience, computational modeling, neuroimaging, and related approaches
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to the Research Manager, the Research Coordinator provides professional-level support for clinical, biomedical, and behavioral research studies involving human participants. The position coordinates study
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Department: RI Office of Clinical Trials Administration (OCTA) ----- Clinical Research Management Department Position Title: Portfolio Manager - Research Administration Job Family Group
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, Clinical Research Center personnel, UNeHealth/SPA, accounting and IRB personnel to ensure optimal outcomes. Directs the research study team. Position Details Additional Information Posting Category
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during course and at the close of the study. Represents the research program at meetings, national and international research consortia. Prepares, submits and maintains IRB, FDA, NCI, NIH, NSF and/or other