Clinical Research Coordinator

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 participate in research conducted by the Division of Gastroenterology in the Department of Medicine under the supervision of the Principal Investigators PIs of the Gastroenterology Research Program. This CRP will perform a variety of research and duties including consenting, enrollment, conducting subject visits, study and site documentation, data entry etc in compliance with sponsor, regulatory, and institutional guidelines, collaborating with physicians and nurses/clinic staff to obtain the specimen, processing/management/shipment of samples to support the conduct of clinical research. Other tasks may include EMR review, participant screening, IP management, query resolution and participant payment processing. The CRP will be integrated into a larger clinical research team and is expected to collaborate on studies that will further the research mission of the Gastroenterology program. This position reports to the CRC Sr..The Principal Investigators 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 Duke Health; perform a variety of duties involved in the collection, compilation, documentation, and analysis of clinical research data. May oversee the work of junior staff and train or mentor others in clinical research




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