2010 -2012 Clinical Development and Regulatory Affairs Fellow @
2006 -2008 Regulatory Affairs Intern @
2000 -2006 Clinical Research Coordinator @
1999 -2000 Clinical and Behavioral Data Specialist @ Marcus Autism Center
1998 -1999 Research Assistant @ Institute for Biological Detection Services
Kerri Kaplan Education
St. John's University
Post-Doctoral Fellowship (Clinical Development and Regulatory Affairs)
2010-2012
Long Island University
PharmD (Pharmacy)
2006-2010
Auburn University
B.A. (Psychology)
1999
Kerri Kaplan Skills
Regulatory Affairs
Clinical Research
Regulatory Submissions
Clinical Development
Pharmaceutical Industry
Clinical Trials
IND
FDA
Drug Development
Regulatory Requirements
CRO
eCTD
Pharmacists
Life Sciences
Pharmaceutics
Therapeutic Areas
CRO Management
GCP
Electronic Common Technical Document (eCTD)
Good Clinical Practice (GCP)
Regulatory
Research
Quality Assurance
Good Clinical Practice Gcp
u.s. Food and Drug Administration Fda
Electronic Common Technical Document Ectd
u.s. Food and Drug Administration
Electronic Common Technical Document
Good Clinical Practice
Kerri Kaplan Summary
Kerri Kaplan, based in New York, United States, is currently a Executive Director, Therapeutic Area Lead at Biogen. Kerri Kaplan brings experience from previous roles at Biogen, AbbVie and Allergan. Kerri Kaplan holds a 2010 - 2012 Post-Doctoral Fellowship in Clinical Development and Regulatory Affairs @ St. John's University. With a robust skill set that includes Regulatory Affairs, Clinical Research, Regulatory Submissions, Clinical Development, Pharmaceutical Industry and more. Kerri Kaplan has 4 emails and 1 mobile phone numbers on RocketReach.
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