2001 -2007 Sr. Director of Regulatory Affairs @ Forest Research Institute
Doreen Morgan Education
St. John's University
Pharm.D., M.S., B.S., RPh. (pharmacy)
Doreen Morgan Skills
Regulatory Affairs
Regulatory Submissions
Clinical Development
NDA
IND
Drug Development
Drug Safety
Pharmacovigilance
eCTD
Medical Affairs
Clinical Trials
GCP
Regulatory Requirements
CRO
FDA
Therapeutic Areas
Pharmaceutical Industry
Medical Writing
CMC
Sop
Biopharmaceuticals
CTMS
21 CFR Part 11
Oncology
GxP
Clinical Pharmacology
Biologics
Pharmacology
Pharmacokinetics
GLP
Pharmaceutics
Clinical Trial Management System Ctms
Good Laboratory Practice Glp
Good Clinical Practice Gcp
CRO Management
Marketing
Customer Service
U.S. Food And Drug Administration Fda
Electronic Common Technical Document Ectd
Standard Operating Procedure Sop
New Drug Application Nda
Safety Management Systems
Research
Good Clinical Practice
New Drug Application
u.s. Food and Drug Administration
Electronic Common Technical Document
Standard Operating Procedure
Clinical Trial Management System
Good Laboratory Practice
Doreen Morgan Summary
Doreen Morgan, based in Chatham, NJ, US, is currently a Vice President Regulatory Affairs at Pfizer. Doreen Morgan brings experience from previous roles at Metsera, Anthos Therapeutics a Novartis company, Self-employed and PTC Therapeutics, Inc.. Doreen Morgan holds a Pharm.D., M.S., B.S., RPh. in pharmacy @ St. John's University. With a robust skill set that includes Regulatory Affairs, Regulatory Submissions, Clinical Development, NDA, IND and more. Doreen Morgan has 6 emails and 1 mobile phone numbers on RocketReach.
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