1999 -
2000 Publishing Specialist @ Wyeth-Ayerst Research
1997 -
1998 Regulatory Document Coordinator @ Astra Merck Inc.
James Mann Skills
eCTD
IND
Regulatory Submissions
Regulatory Affairs
FDA
Pharmaceutical Industry
GMP
Clinical Development
Biotechnology
Oncology
21 CFR Part 11
Regulatory Requirements
Sop
Validation
Clinical Trials
Pharmacovigilance
Computer System Validation
Quality Assurance
Medical Writing
GxP
GLP
GCP
U.S. Food and Drug Administration (FDA)
Standard Operating Procedure (SOP)
Publishing
U.S. Food And Drug Administration Fda
Standard Operating Procedure Sop
Research
Computer System
Electronic Common Technical Document Ectd
Standard Operating Procedure
u.s. Food and Drug Administration
Electronic Common Technical Document
James Mann Summary
James Mann, based in King of Prussia, PA, US, is currently a Director, Regulatory Affairs, Operations and Submissions at Inovio Pharmaceuticals Inc.. James Mann brings experience from previous roles at TissueTech, Inc, Braeburn, Teva Pharmaceuticals and Cephalon. With a robust skill set that includes eCTD, IND, Regulatory Submissions, Regulatory Affairs, FDA and more. James Mann has 2 emails and 2 mobile phone numbers on RocketReach.
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