Diane Stroehmann Email & Phone Number
Senior Vice President, Regulatory Affairs @ Viridian Therapeutics, Inc.
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Diane Stroehmann Location
- Boston, MA, US
Diane Stroehmann Work
- Senior Vice President, Regulatory Affairs @ (June 2024 - Present)
- Chief, Member @ (February 2021 - June 2024)
- Vice President Regulatory Affairs and Global Patient Safety @ (August 2019 - June 2024)
- Chief of Staff; Vice President and Head of Regulatory Affairs and Quality @ (January 2016 - July 2019)
- Vice President, Regulatory Affairs, Pharmacovigilance and Research Compliance @ KYTHERA Biopharmaceuticals (September 2013 - October 2015)
- Executive Director, Regulatory Affairs @ (February 2010 - August 2013)
- Associate Director, Regulatory Affairs @ (October 2008 - March 2010)
- Manager, Regulatory Affairs @ (March 2004 - October 2008)
- Regulatory Affairs Specialist @ Organics/LaGrange Inc. (January 2002 - January 2004)
- Clinical Research Associate @ (January 2001 - January 2002)
- Clinical Research Assistant @ (January 1999 - January 2001)
Diane Stroehmann Education
- University of Illinois Urbana-Champaign
BS (Biology)
- San Diego State University
MS (Regulatory Affairs)
Diane Stroehmann Skills
- 21 CFR Part 11
- Biologics
- Biotechnology
- CAPA
- CMC
- CRO
- CTMS
- Change Control
- Clinical Development
- Clinical Research
- Clinical Trial Management System (CTMS)
- Clinical Trials
- Dermatology
- Drug Development
- FDA
- GCP
- GLP
- GMP
- Good Clinical Practice (GCP)
- Good Laboratory Practice (GLP)
- IND
- Life Sciences
- Lifesciences
- Medical Affairs
- Medical Devices
- Pharmaceutical Industry
- Pharmaceutics
- Pharmacovigilance
- Regulations
- Regulatory Affairs
- Regulatory Requirements
- Regulatory Submissions
- SOP
- Standard Operating Procedure (SOP)
- Technology Transfer
- U.S. Food and Drug Administration (FDA)
- U.S. Title 21 CFR Part 11 Regulation
- eCTD
- Strategy
- Sales
- Business Development
- Clinical Trial Management System Ctms
- Good Laboratory Practice Glp
- Good Clinical Practice Gcp
- u.s. Food and Drug Administration Fda
- Standard Operating Procedure Sop
- u.s. Food and Drug Administration
- Standard Operating Procedure
- Good Clinical Practice
- Good Laboratory Practice
- Clinical Trial Management System
Diane Stroehmann Summary
- Diane Stroehmann, based in Boston, MA, US, is currently a Senior Vice President, Regulatory Affairs at Viridian Therapeutics, Inc.. Diane Stroehmann brings experience from previous roles at Chief, Ironwood Pharmaceuticals, Sienna Biopharmaceuticals and KYTHERA Biopharmaceuticals. Diane Stroehmann holds a BS in Biology @ University of Illinois Urbana-Champaign. With a robust skill set that includes 21 CFR Part 11, Biologics, Biotechnology, CAPA, CMC and more. Diane Stroehmann has 2 emails and 3 mobile phone numbers on RocketReach.
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Top Viridian Therapeutics, Inc. Employees
Diane Stroehmann
Senior Vice President, Regulatory Affairs
Boston, MA, US
Steve Mahoney
President and Chief Executive Officer
Boston, MA, US
Craig Flanagan
Vice President, Sales and Marketing
Pittsburgh, PA, US
Seth Harmon
Chief Financial Officer
Boston, MA, US
Seong Han
Senior Vice President, Pharmacovigilance
Princeton, NJ, US
Jennifer Sheng
VP, Head of Clinical Pharmacology and Pharmacometrics
Princeton, NJ, US
Kirk Bertelsen
Sr. Vice President, Head of Research
Doylestown, PA, US
Jeremy Brinkerhoff
Vice President, Finance
Boston, MA, US
Christine Waite
VP, Marketing TED
Cambridge, MA, US
Chad Morin
Senior Vice President, Chief Compliance Officer
Boston, MA, US
Tony Casciano
Chief Commercial Officer (CCO)
Boston, MA, US
Radhika Tripuraneni
Chief Medical Officer
California, United States
Daniel Alvarez
Vice President Clinical Development
Wynnewood, PA, US
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