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Associate Director of Clinical Trials
Reporting to the Director of Clinical Research for the RadOnc CRU, the Associate Director of Clinical Research will be primarily responsible for the daily research operations and for the overall education and training program for the CRU staff and investigators to support the conduct of cancer clinical trials. Additional responsibilities include day-to-day quality assurance oversight in alignment with ICH Good Clinical Practice (GCP) to ensure CRU inspection readiness and compliance with the requirements of the University of Pennsylvania, FDA, and all applicable regulatory bodies. The candidate must have a thorough knowledge of ICH-GCP regulations and a comprehensive understanding of clinical trial processes, and the conduct of clinical research studies.


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