Karl Whitney,, PhD, SVP Global Regulatory Affairs
Karl Whitney, Ph.D., RAC joined Passage in February 2024 as Senior Vice President, Global Regulatory Affairs. Dr. Whitney has 25 years’ experience in the pharmaceutical industry, specializing in regulatory strategy, clinical regulatory affairs, and integrated product development. From early 2020 to 2024, he led the regulatory function at Precision BioSciences (Durham, NC) as Vice President and Head of Regulatory Affairs, responsible for regulatory strategy, execution, and operations for all of Precision's oncology cell therapy and in vivo genome editing programs. Prior to Precision, Dr. Whitney spent 10 years at Rho, Inc., a full-service CRO where he managed, led, and guided numerous regulatory submission and development projects across a range of therapeutic areas and development stages, in addition to overseeing clinical trial projects and helping establish a regulatory strategy training program for Ph.D. scientists entering the pharmaceutical industry. Dr. Whitney currently also serves as co-President of the International FOXP1 Foundation, an ultrarare genetic neurodevelopmental disorder, and as an advisor to the UNC Eshelman School of Pharmacy's Master of Professional Science degree in Regulatory Science. Dr. Whitney received his undergraduate degree from Yale and a Ph.D. in pharmacology from Duke.