Scott Korn M.D.

Scott Korn, M.D., has more than 30 years of global regulatory and drug development experience. He has provided strategic regulatory leadership at all phases of drug development for small molecules and biologics, with a successful track record of numerous submissions and approvals in multiple therapeutic areas. Dr. Korn began his biopharma industry career at Merck Research Laboratories, where he continues to work today. He has held roles in clinical research, drug safety and regulatory affairs. He served as vice president of Global Regulatory Affairs for general medicine and currently holds that position for oncology and in vitro diagnostics. Dr. Korn has extensive experience interacting with the United States Food and Drug Administration, the European Medicines Agency and other leading regulatory agencies.