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. Be You. At Duke, we celebrate individuality and the unique perspectives that each member of our community brings. As a Clinical Research Coordinator II, you will play a critical role in advancing innovative research focused on memory disorders and movement disorders. Working alongside physicians, neuroscientists, research participants, and multidisciplinary stakeholders, you will help drive complex clinical studies that improve patient outcomes and contribute to groundbreaking scientific discoveries. You will join a collaborative and mission-driven environment where your expertise in clinical research operations, participant engagement, regulatory compliance, and data management will directly contribute to the advancement of neuroscience research. Be Bold. Join a research team dedicated to improving the lives of individuals affected by cognitive and neurological disorders. In this role, you will independently coordinate complex clinical studies while serving as a trusted resource for investigators, participants, sponsors, and research staff. What You'll Do: Clinical Research Operations Coordinate and manage complex clinical research studies from activation through closeout. Maintain study documentation, regulatory files, standard operating procedures SOPs, and participant records. Manage investigational products, including receipt, storage, accountability, tracking, and participant distribution. Serve as the primary liaison between study sponsors, Investigational Drug Services IDS, regulatory offices, and research teams. Support study monitoring visits, audits, and inspections, ensuring timely resolution of findings and compliance requirements. Develop workflows, operational resources, and tools that enhance research efficiency and study execution. Participant Recruitment & Retention Screen, enroll, and retain research participants for procedural, interventional, and greater-than-minimal-risk studies. Conduct informed cons
