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Sarah Cannon Research Institute

Clinical Trials Protocol Coordinator

Sarah Cannon Research Institute, Nashville, Tennessee, United States

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A leading oncology research institute in Tennessee seeks a Research Protocol Coordinator to manage and support research initiatives within the department. The role involves extensive oncology knowledge, coordination of clinical trial operations, and compliance with federal regulations. Candidates should hold an Associate’s Degree, preferably with experience in Clinical Trial Management Systems. Join a mission-driven team focused on improving cancer patient outcomes. Competitive compensation and comprehensive benefits package offered. #J-18808-Ljbffr