Mark De Rosch, PhD, FRAPS
Executive Vice President, Regulatory and Government Affairs, and Program Management
Dr. De Rosch is an experienced executive pharma/biotech leader (30+ years) mostly with organizations transitioning from early- to late-stage development and to commercialization. He joined CervoMed Inc. in November 2024 as Senior Vice President, Regulatory and Government Affairs, and Program Management and became Executive Vice President in May 2025. Prior to joining CervoMed, He consulted on drug development and global regulatory strategies since May 2023. Previously Dr. De Rosch was Chief Operating Officer at Aura Biosciences from March 2021 to May 2023 overseeing Regulatory Affairs, CMC / Technical Operations, Program & Portfolio Management, Medical Device Innovation, and Information Technology (IT). While at Aura, he contributed to Aura becoming a public company and growing from about 20 employees to about 65 employees to support Phase 3 readiness. Prior to joining Aura, Dr. De Rosch was Chief Regulatory Officer at Epizyme, Inc. where he assisted Epizyme in receiving Accelerated Approval in the US for its first drug, TAZVERIK®, in 2 oncology indications. Prior to Epizyme, he was Senior Vice President of Regulatory, Quality, and Medical Writing at Nightstar Therapeutics, Inc., a gene therapy company specializing in treatment of inherited retinal disease that was acquired by Biogen in 2019. Prior organizations include Akebia Therapeutics, Voisin Consulting Life Sciences, Inspiration Biopharmaceuticals, Vertex Pharmaceuticals, Berlex Laboratories, Diatide, and Mallinckrodt.
He was designated as a Fellow of the Regulatory Affairs Professional Society (FRAPS) in 2017.