Allison Bohren Email & Phone Number
Senior Manager, Regulatory Affairs @ Defibtech, LLC
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Allison Bohren Location
- Guilford, CT, US
Allison Bohren Work
- Senior Manager, Regulatory Affairs @ (June 2025 - Present)
- Manager, Regulatory Affairs @ (March 2023 - June 2025)
- Senior Regulatory Affairs Specialist @ (October 2020 - March 2023)
- Assistant Director, Regulatory Affairs at Yale Cancer Center @ (May 2018 - October 2020)
- Senior Manager, Global Regulatory Affairs @ (February 2016 - May 2018)
- Senior Manager, Global Regulatory Affairs @ (June 2015 - January 2016)
- Manager, Regulatory Affairs @ (December 2013 - June 2015)
- Contractor - Regulatory Affairs Submissions Manager @ (September 2012 - December 2013)
- 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
- Northeastern University
M.S. (Regulatory Affairs)
- University of Connecticut
B.S. (Molecular and Cell Biology, Psychology)
Allison Bohren Skills
- ANDA
- Assay Development
- Biopharmaceuticals
- Biotechnology
- CAPA
- CMC
- CRO
- CRO Management
- Clinical Development
- Clinical Trials
- Corrective and Preventive Action (CAPA)
- Drug Development
- ELISA
- Electronic Common Technical Document (eCTD)
- Electronic Submissions
- FDA
- GCP
- GLP
- GMP
- Good Clinical Practice (GCP)
- Good Laboratory Practice (GLP)
- IND
- Life Sciences
- Lifesciences
- Medical Devices
- NDA
- PMA
- Pharmaceutical Industry
- Pharmaceutics
- Pharmacokinetics
- Pharmacology
- Protein Chemistry
- Regulatory Affairs
- Regulatory Documentation
- Regulatory Requirements
- Regulatory Submissions
- SOP
- Standard Operating Procedure (SOP)
- U.S. Food and Drug Administration (FDA)
- Validation
- eCTD
- Good Laboratory Practice Glp
- Good Clinical Practice Gcp
- Corrective and Preventive Action Capa
- Electronic Common Technical Document Ectd
- 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 M.S. in Regulatory Affairs @ Northeastern University. With a robust skill set that includes ANDA, Assay Development, Biopharmaceuticals, Biotechnology, CAPA and more. Allison Bohren has 4 emails and 2 mobile phone numbers on RocketReach.
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