Regulatory Affairs Specialist @ (January 2011 - September 2012)
Regulatory Affairs Associate II @ (September 2008 - January 2011)
Regulatory Affairs Associate @ (February 2007 - August 2008)
Assistant Research Scientist @ (September 2005 - February 2007)
Allison Bohren Education
University of Connecticut
B.S. (Molecular and Cell Biology, Psychology)
Northeastern University
M.S. (Regulatory Affairs)
Allison Bohren Skills
Clinical Trials
Good Laboratory Practice Glp
CRO
ELISA
GMP
eCTD
Regulatory Documentation
Assay Development
Good Clinical Practice Gcp
Biotechnology
Regulatory Affairs
IND
Life Sciences
Validation
Medical Devices
Corrective and Preventive Action Capa
Regulatory Requirements
Lifesciences
CRO Management
NDA
PMA
GCP
Pharmaceutics
Clinical Development
Drug Development
Regulatory Submissions
ANDA
Pharmacology
CMC
Electronic Common Technical Document Ectd
Pharmaceutical Industry
GLP
CAPA
FDA
Sop
Protein Chemistry
Pharmacokinetics
Biopharmaceuticals
Electronic Submissions
Electronic Common Technical Document
Good Laboratory Practice
Corrective and Preventive Action
Good Clinical Practice
Allison Bohren Summary
Allison Bohren, based in Guilford, CT, US, is currently a Senior Manager, Regulatory Affairs at Defibtech, LLC. Allison Bohren brings experience from previous roles at Defibtech, LLC, Yale University School of Medicine and Vertex Pharmaceuticals. Allison Bohren holds a B.S. in Molecular and Cell Biology, Psychology @ University of Connecticut. With a robust skill set that includes Clinical Trials, Good Laboratory Practice Glp, CRO, ELISA, GMP and more. Allison Bohren has 4 emails and 2 mobile phone numbers on RocketReach.
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