Navigating Research Protections Series - Session 2: Study Design and Clinical Protocol Development

Join us for the second session of our Navigating Research Protections Series, where we explore key aspects of designing research projects and developing clinical protocols. Richard Sucgang, PhD, Scientist, Center for Health Data Science and Analytics, will provide an overview of the foundational principles and practical considerations in study design, including common design strategies for translating scientific questions into robust research projects. Susan Miller, MD, MPH, FACP, FAAFP, Professor, Clinical Family Medicine, and former Senior Chair of the Institutional Review Board, will discuss the critical components of clinical protocols and the underlying rationale for them, and the oversight of study execution.

Offered by the Office of Faculty and Research Development and the Office of Research Protections