Diane Marie Stroehmann

age ~46

from Simi Valley, CA

Also known as:
  • Diane M Stroehmann
  • Diane S Stroehmann
  • Diane Marie Deegan
  • Diane M Stroehman
  • Diane M Deegan

Diane Stroehmann Phones & Addresses

  • Simi Valley, CA
  • Agoura Hills, CA
  • Gilbert, AZ
  • Schaumburg, IL
  • Elk Grove Village, IL
  • Natick, MA
  • Maricopa, AZ
  • Scottsdale, AZ
  • 29902 Rainbow Crest Dr, Agoura Hills, CA 91301

Work

  • Company:
    Ironwood pharmaceuticals
    Aug 2019
  • Position:
    Vice president regulatory affairs and global patient safety

Education

  • Degree:
    Master of Science, Masters
  • School / High School:
    San Diego State University
    2007 to 2010

Skills

Regulatory Affairs • Regulatory Submissions • Fda • Pharmaceutical Industry • Clinical Research • Ind • Clinical Development • Biotechnology • Clinical Trials • Pharmacovigilance • Drug Development • Medical Devices • Medical Affairs • Gcp • Pharmaceutics • Dermatology • Regulatory Requirements • Gmp • Sop • Ectd • Glp • U.s. Food and Drug Administration • Cro • Biologics • Cmc • Regulations • Technology Transfer • Life Sciences • 21 Cfr Part 11 • Lifesciences • Change Control • Ctms • Capa • Standard Operating Procedure • Good Clinical Practice • Good Laboratory Practice • Clinical Trial Management System

Industries

Pharmaceuticals

Resumes

Diane Stroehmann Photo 1

Vice President Regulatory Affairs And Global Patient Safety

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Location:
217 Mill Ct, Simi Valley, CA 93065
Industry:
Pharmaceuticals
Work:
Ironwood Pharmaceuticals
Vice President Regulatory Affairs and Global Patient Safety

Sienna Biopharmaceuticals
Chief of Staff; Head of Regulatory Affairs and Quality

Kythera Biopharmaceuticals Sep 2013 - Oct 2015
Vice President, Regulatory Affairs, Pharmacovigilance and Research Compliance

Medicis Feb 2010 - Aug 2013
Executive Director, Regulatory Affairs

Medicis Oct 2008 - Mar 2010
Associate Director, Regulatory Affairs
Education:
San Diego State University 2007 - 2010
Master of Science, Masters
University of Illinois at Urbana - Champaign 1995 - 1999
Bachelors, Bachelor of Science, Biology
Skills:
Regulatory Affairs
Regulatory Submissions
Fda
Pharmaceutical Industry
Clinical Research
Ind
Clinical Development
Biotechnology
Clinical Trials
Pharmacovigilance
Drug Development
Medical Devices
Medical Affairs
Gcp
Pharmaceutics
Dermatology
Regulatory Requirements
Gmp
Sop
Ectd
Glp
U.s. Food and Drug Administration
Cro
Biologics
Cmc
Regulations
Technology Transfer
Life Sciences
21 Cfr Part 11
Lifesciences
Change Control
Ctms
Capa
Standard Operating Procedure
Good Clinical Practice
Good Laboratory Practice
Clinical Trial Management System

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