Peggy Morris Charpie

Peggy Morris Charpie currently holds the position of Acting VP and Head of US Regulatory Affairs at ONO PHARMA USA, where responsibilities include managing strategic engagements with project leaders and FDA officials, as well as developing regulatory strategies for product approvals. Previous experience includes serving as Senior Director of Regulatory Affairs at ONO PHARMA USA and Director of Regulatory Affairs at Seqirus, where Peggy also acted as Interim Head of North America Regulatory Affairs. Peggy's extensive background in regulatory affairs spans multiple roles, including Associate Director of Global Regulatory Affairs at Takeda Pharmaceuticals, Associate Director of International Regulatory Affairs at Millennium Pharmaceuticals, and various managerial positions in clinical trials and project management across several organizations. Peggy holds an MS in Clinical Research Design and Statistical Analysis from the University of Michigan and a BSN in Nursing from Northeastern University.