Ashish Chavda Email
Associate Director - Global Regulatory Lead @ Bristol Myers Squibb
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Ashish Chavda Work
- 2026 -now Associate Director - Global Regulatory Lead @
- 2024 -2025 Associate Director, Head of RA Semaglutide and GLP-1 @
- 2022 -2024 Global Program Regulatory Manager (GPRM) @
- 2020 -2022 GPRM (on Job Rotation) @
- 2017 -2022 Manager - RA Global Drug Development @
- 2008 -2017 Manager @
- 2008 -2011 Regulatory Affairs Executive @ Invida India Pvt Ltd
Ashish Chavda Education
- Harvard Medical School
Certification Course (Drug Discovery and Development (HMX Pro))
2025-2025 - Harvard Medical School
Certification Course (Clinical Drug Development: Clinical Trial Methodologies and Innovations)
2024-2024 - Harvard Medical School
Certification Course (Foundational Concepts in Pharmacology)
2024-2024 - Massachusetts College of Pharmacy and Health Sciences
Master of Science - MS (Regulatory Affairs and Health Policy)
2021-2022 - Institute of Clinical Research (India), Ahmedabad
PGD in Advanced Clinical Research (Clinical Research)
2007-2008 - Hemchandracharya North Gujarat University
Master of Science (M.Sc.) (Microbiology, General)
2004-2006 - Sainik School Balachadi
(CBSE Board)
2000-2001
Ashish Chavda Summary
- Ashish Chavda, is currently a Associate Director - Global Regulatory Lead at Bristol Myers Squibb. Ashish Chavda brings experience from previous roles at Novo Nordisk and Novartis. Ashish Chavda holds a 2025 - 2025 Certification Course in Drug Discovery and Development (HMX Pro) @ Harvard Medical School. Ashish Chavda has 3 emails on RocketReach.
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