Director, Project Management, Regulatory Affairs. Manager, Business Development @ Esperion Therapeutics
Project Manager @ i3 Statprobe
Regulatory Affairs, Drug Safety Associate @ Parke-Davis Pharmaceutical Research
Peggy Charpie's Education
University of Michigan
MS (Clinical Research Design and Statistical Analysis)
1997 - 1999
Northeastern University
BSN (Nursing)
1978 - 1986
Peggy Charpie's Skills
Contingency Planing (regulatory affairs related)
Writing (regulatory, scientific, strategic)
Strategic Planning
Business Strategy
Excellent Communication (written and oral)
Microsoft Office
Mac or PC
Clinical Research
Global Drug Development
EU Centralised Submissions
Peggy Charpie's Summary
Peggy Charpie, based in Cambridge, MA, US, is currently a Senior Director Regulatory Affairs at ONO PHARMA USA, bringing experience from previous roles at Seqirus, Takeda Pharmaceuticals International, Millennium Pharmaceuticals and Repligen Corporation and Repligen Europe Limited. Peggy Charpie holds a 1997 - 1999 MS in Clinical Research Design and Statistical Analysis @ University of Michigan. With a robust skill set that includes Contingency Planing (regulatory affairs related), Writing (regulatory, scientific, strategic), Strategic Planning, Business Strategy, Excellent Communication (written and oral) and more, Peggy Charpie contributes valuable insights to the industry. Peggy Charpie has 2 emails and 1 mobile phone number on RocketReach.