Megan Crilly

Megan Crilly is an accomplished professional in CMC Regulatory Affairs with extensive experience at Regeneron since September 2016, progressing from CMC Regulatory Affairs Specialist to Associate Director. Responsibilities include preparing and reviewing various documents to support clinical drug development and ensuring compliance with product life cycle documentation. Megan is a registered member of MTOPRA and an active participant in the Regulatory Affairs Professionals Society (RAPS). Earlier experiences include academic roles at the University of Pittsburgh, where teaching and research contributions focused on public health and drug education. Megan holds a Master’s Degree in Health Policy and Economics from the University of Pittsburgh and a Bachelor’s Degree in the History of Science and Medicine from the University of Rochester.