Faculty Development Seminar Series: Writing Clinical Research Protocols

Presented by Matthew Exline, MD, Professor College of Medicine and Ellen Patricia, MS, Director of the Office of Responsible Research Practices

This seminar offers a practical introduction to the development of clinical research protocols, equipping investigators and research staff with the tools to design clear, compliant and scientifically sound studies. Participants will explore the essential components of a clinical protocol, including study objectives, methodology, eligibility criteria, data collection plans and ethical considerations. The session will also address regulatory expectations, Institutional Review Board (IRB) requirements and best practices for protocol formatting and submission.