Debra Feldman's Location
Needham, MA, US
Debra Feldman's Work
- Chief Regulatory Affairs Officer @ Dyne Therapeutics
- Senior Vice President Regulatory Affairs @ Dyne Therapeutics
- VP Regulatory Affairs @ Dyne Therapeutics
- Vice President Regulatory Affairs @ Sage Therapeutics
- Senior Director Regulatory Affairs @ Sage Therapeutics
- Senior Director Regulatory Affairs @ Medivector Inc
- Independent Regulatory Consultant @ DB Feldman Consulting
- Independent Regulatory Affairs Consultant @ Pfizer
- Regulatory Affairs Consultant @ Artisan Pharma
- Director of Regulatory Affairs @ AMAG Pharmaceuticals
Debra Feldman's Education
- Boston University
MPH (Masters in Public Health)
1999 - 2003 - University of Massachusetts Amherst
Bachelors
Debra Feldman's Skills
- Pharmaceutical Industry
- Clinical Development
- Regulatory Affairs
- Clinical Trials
- FDA
- Biotechnology
- Clinical Research
- Lifesciences
- Drug Development
- CMC Regulatory Affairs
Debra Feldman's Summary
Debra Feldman, based in Needham, MA, US, is currently a Chief Regulatory Affairs Officer at Dyne Therapeutics, bringing experience from previous roles at Dyne Therapeutics, Sage Therapeutics and SAGE Therapeutics. Debra Feldman holds a 1999 - 2003 MPH in Masters in Public Health @ Boston University. With a robust skill set that includes Pharmaceutical Industry, Clinical Development, Regulatory Affairs, Clinical Trials, FDA and more, Debra Feldman contributes valuable insights to the industry. Debra Feldman has 3 emails on RocketReach.
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