2002 -2004 Regulatory Affairs Specialist @ Organics/LaGrange Inc.
2001 -2002 Clinical Research Associate @
1999 -2001 Clinical Research Assistant @
Diane Stroehmann Education
University of Illinois Urbana-Champaign
BS (Biology)
San Diego State University
MS (Regulatory Affairs)
Diane Stroehmann Skills
Regulatory Submissions
Clinical Development
Strategy
CRO
Life Sciences
Pharmacovigilance
Clinical Research
Sales
Technology Transfer
Pharmaceutical Industry
Business Development
21 CFR Part 11
Clinical Trials
CAPA
Regulatory Affairs
Dermatology
Biologics
Drug Development
eCTD
GMP
CMC
GLP
Biotechnology
FDA
IND
Lifesciences
Medical Affairs
Pharmaceutics
GCP
CTMS
Medical Devices
Regulatory Requirements
Sop
Change Control
Regulations
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 Regulatory Submissions, Clinical Development, Strategy, CRO, Life Sciences and more. Diane Stroehmann has 2 emails on RocketReach.
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