Robert Charnas, PhD
Robert Charnas, PhD is a pharmaceutical executive with over 20 years of global regulatory and strategic program leadership experience. He has a proven track record in successful product registrations for both small and large molecules across North America, Europe, and Asia. His expertise spans development from pre-IND through Phase IV studies, with a strong focus on oncology, infectious diseases, and experience in rare diseases. He most recently served as Worldwide Regulatory Affairs Transformation Lead and Head of US Regulatory Affairs at Servier Bio-Innovation, where he oversaw key regulatory successes, including the FDA approval of VORANIGO for IDH-mutant low-grade glioma and TIBSOVO for both 1L ICIE AML (in combination with azacitidine) and R/R MDS. Previously, Dr. Charnas was Vice President and Head of Global Regulatory Affairs at Agios Pharmaceuticals and Vice President of Strategic Program Direction for Oncology at Regeneron Pharmaceuticals.
He has also worked at top pharmaceutical companies, including Amgen, Novartis, and Hoffmann-La Roche, having had functions in regulatory affairs, clinical development, and medical strategy. A Harvard-trained Ph.D. chemist with prestigious fellowships and honors, including the Johnson Medal at J&J, Dr. Charnas is a multilingual leader adept at fostering innovation in drug development.