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. This full-time onsite Clinical Research Professional CRP will serve as the primary coordinator for assigned clinical research studies and will support the Lead in managing the study portfolio for research conducted by the Division of Endocrinology in the Department of Medicine under the supervision of the Principal Investigators PIs. The CRP will be responsible for a broad range of clinical research activities, including participant recruitment, screening, informed consent, enrollment, coordination and conduct of study visits, maintenance of study and site documentation, and data entry. All activities will be conducted in compliance with sponsor, regulatory, and institutional guidelines. Other tasks include EMR review, collection/processing/shipment of research specimen, investigational product IP management, query resolution, participant payment processing, workflow coordination and ongoing communication with investigators, sponsors, and organizational leadership. The ideal candidate will be highly organized, detail-oriented, and adaptable, with demonstrated ability to manage multiple priorities and stakeholders independently. Prior Duke clinical trial experience is preferred. This position will report to the CRC, Sr.. The PIs will provide supervision, regulatory oversight, mentorship, and guidance in the conduct of research. Minimum Requirements: Education/Training Completion of an Associate's degree Experience Work requires a minimum of two years of relevant research experience. Completion of the DOCR North Carolina state approved Clinical Research Apprenticeship program may substitute for one year of required experience. Skills Can easily use computing software and web based applications e.g., Microsoft Office products and internet browsers. This position is: Onsite Be Bold. As a Clinical Research Coordinator you will participate in or lead day to day operations of clinical research studies conducted by Principal Investigators PI at
