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. Be Bold. Choose Duke. Clinical Research Coordinator II Be You. At Duke Health, we celebrate individuality, curiosity, and the unique experiences that every team member brings to advancing discovery and improving patient care. As a Clinical Research Coordinator II, you will play a critical role in supporting innovative clinical research studies while partnering with investigators, research participants, sponsors, and interdisciplinary teams. Your expertise will help ensure studies are conducted ethically, efficiently, and in compliance with regulatory requirements. You will join a collaborative research environment where your contributions directly support groundbreaking discoveries that improve health outcomes and impact lives locally and globally. Be Bold. As a Clinical Research Coordinator II, you'll independently manage and coordinate complex clinical research activities, ensuring excellence in participant safety, regulatory compliance, data integrity, and study operations. What You'll Do: Lead Research Operations Coordinate day-to-day activities for clinical research studies, including studies involving greater than minimal risk and complex interventions. Manage all aspects of investigational products, including receipt, storage, tracking, accountability, and participant dispensing. Serve as a primary liaison among sponsors, investigators, regulatory offices, research support services, and study teams. Prepare and maintain study documentation, regulatory files, standard operating procedures, and protocol submissions. Support study monitoring visits, audits, inspections, and closeout activities while addressing findings and implementing corrective actions. Coordinate participant recruitment, screening, enrollment, retention, and study visit activities. Collect, process, maintain, and ship research specimens according to protocol and regulatory requirements. Advance Participant Safety and Research Ethics Conduct informed consent discussions and d
