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. Work under close direction of the principal investigator and/or study coordinator/supervisor. Duties include: Serve as primary contact with research participants, sponsors, and regulatory agencies
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questionnaires. Perform clerical duties in the preparation of regulatory documents. Maintain all forms and documents, including consent forms and master subject logs. File all appropriate correspondence. Assist
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consent forms and master subject logs. File all appropriate correspondence. Assist in the preparation and publication of research abstracts and manuscripts by working with biostatisticians, residents, and
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Coordinator who will be assigned to multiple clinical trial under the direction of the Principal Investigator and will work closely with the Amyloid Center Research Team. The clinical trials
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consent forms and master subject logs. File all appropriate correspondence. Assist with the screening, recruiting, and obtaining consent of study participants. Review medical records and/or perform
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collaboration with the principal investigator, study investigators and an interdisciplinary team, and manage clinical research coordinators on the studies. Members of the Center possess deep domain experience in
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hand with Principal Investigators, Clinical Research [Nurse] Managers, Associates and other stakeholders in support of patients with Heart Transplantation and Heart Failure. Duties include: Schedule and
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include*: Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out. Determine eligibility of and gather consent from study
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for renewal based on funding availability. To learn more about the lab and PI , please visit: https://med.stanford.edu/pans.html The Immune Behavioral Health/PANS Research Program within the Department
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regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to requests and questions. Collaborate with principal