The Clinical Research Coordinator will manage activities in the data coordinating center for an established large multicenter trial of a diet intervention. In addition, this position will manage regulatory compliance for two national multicenter studies that includes the development of IRB reliance agreements, oversight of regulatory compliance at sites operating under their own IRB as well as the central IRB at Penn, and training of external site coordinators regarding regulatory compliance. Other responsibilities include: monitoring and reporting on study progress, acting as a central point of contact for clinical site coordinators around the country, managing vendor relationships including invoicing and problem resolution, and drafting of all reports and other communications required by the sponsor. This position will also provide patient education, obtain informed consent, implement study procedures and collect biosamples.
Internal Number: 45335
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