Kimberly Koehn, PhD, is a Regulatory Scientist II at Rho since March 2021, leading cross-functional teams on regulatory submission programs and providing technical input for clinical study designs across various therapeutic areas. Previously, Kimberly served as a Regulatory Scientist I and Integrated Product Development Associate, managing project scopes, budgets, and timelines. At the University of North Carolina at Chapel Hill, Kimberly co-chaired a medical and regulatory affairs career club and served as a Postdoctoral Research Associate, managing multi-university projects in drug discovery. Kimberly holds a PhD in Chemistry from Colorado State University and a BS in Chemistry from the College of Charleston.
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