School of Medicine Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive community of outstanding learners, investigators, clinicians, and staff where interdisciplinary collaboration is embraced and great ideas accelerate translation of fundamental scientific discoveries to improve human health locally and around the globe. Composed of more than 2,600 faculty physicians and researchers, nearly 2,000 students, and more than 6,200 staff, the Duke University School of Medicine along with the Duke University School of Nursing, and Duke University Health System comprise Duke Health, a world-class academic medical center. The Health System encompasses Duke University Hospital, Duke Regional Hospital, Duke Raleigh Hospital, Duke Health Integrated Practice, Duke Primary Care, Duke Home Care and Hospice, Duke Health and Wellness, and multiple affiliations. Be You. The Department of Surgery is looking for a Clinical Research Coordinator to join our team. This critical role will participate in the day-to-day operations of clinical research for the Division of Abdominal Transplant. Our patient population are pre- and post-transplant kidney, liver, intestine, and pancreas patients. We work on interventional trials of new drugs, devices, and assays to improve outcomes for all transplant patients. The Surgery Office of Clinical Research SOCR is staffed with experienced individuals who are dedicated to patient safety while conducting innovative research with the hope of advancing medicine and improving clinical care. Minimum Requirements: Completion of an Associate’s Degree A minimum of two years of relevant research experience. A Bachelor’s degree may substitute for two years required experience. Preferred Qualifications: 2–4 years of clinical research experience, preferably within an academic medical center, healthcare system, or clinical research environment. Experience supporting clinical research studies, clinical trials, or research operations. Familiarity with clinical research processes, regulatory requirements, study coordination, and research compliance. Other Requirements: This position is primarily onsite. The ability to come to campus regularly and quickly is required. This position has call responsibilities. Be Bold. Position Description: Knowledgeable in regulatory and institutional policies and processes. Applies knowledge to assist with study documentation, protocol submissions, and standard operating procedures SOPs. Is responsible for all aspects of managing and documenting Investigational Product IP; including arrival, storage, tracking, and provision to research participants. Serves as the primary liaison with sponsors, IDS, and other parties as necessary. Independently employs simple procedures for collecting, preparing, processing, shipping, and maintaining inventory of specimens. Maint
