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

Reports to: Jessica Shier, Research Program Leader, Sr.

Be You.

At Duke, we celebrate individuality and the unique perspectives each team member brings to advancing world-class research. As a Clinical Research Coordinator II, you will play a vital role within one of our pulmonary research clusters, helping to connect innovative research with the patients and communities we serve. You will join a collaborative team dedicated to improving outcomes for individuals with pulmonary and critical illness through groundbreaking clinical research.

Be Bold.

Join a dynamic research environment where you will coordinate complex clinical studies, engage participants throughout their research journey, and contribute to discoveries that have the potential to transform patient care.

What You'll Do

Clinical Research Operations

• Coordinate and manage complex clinical research studies, including procedural and interventional protocols.
• Recruit, screen, consent, enroll, and retain research participants while ensuring compliance with protocol requirements.
• Manage participant scheduling, study visits, randomization activities, and protocol adherence.
• Maintain participant-level and study-level documentation for complex clinical research studies.
• Oversee investigational product (IP) receipt, storage, accountability, tracking, and dispensing activities.
• Prepare studies for monitoring visits, audits, site visits, and closeout activities, addressing findings and implementing corrective actions as needed.