Richard Moscicki

Executive Vice President, Science & Regulatory Advocacy Chief Medical Officer, Pharmaceutical Research and Manufacturers of America

Executive Vice President and Science & Regulatory Advocacy Chief Medical Officer, Pharmaceutical Research and Manufacturers of America

Before joining the Pharmaceutical Research and Manufacturers of America (PhRMA), Moscicki was Deputy Center Director for Science Operations for the U.S. Food and Drug Administration’s (FDA) Center for Drug Evaluation and Research (CDER) since 2013. While at FDA, he brought executive direction of Center operations and leadership in overseeing the development, implementation, and direction of CDER’s programs. Previous positions include serving as Chief Medical Officer at Genzyme Corporation from 1992 to 2011, where he was responsible for worldwide global regulatory and pharmacovigilance matters, as well as all aspects of clinical research and medical affairs for the company. He served as the senior vice president and head of Clinical Development at Sanofi-Genzyme from 2011-2013. He is a member of LogicBio’s board of directors since October 2018. 

Moscicki is board certified in internal medicine, diagnostic and laboratory immunology, and allergy and immunology.