
Msra Saurabh Kothari Msbe Mspm Rph Ccrp Rac
Master's level Regulatory professional with experience in domestic and international regulatory strategy and submissions, TMF Management, and Quality... | Cambridge, Massachusetts, United States
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Msra Saurabh Kothari Msbe Mspm Rph Ccrp Rac’s Emails sk****@no****.edu
Msra Saurabh Kothari Msbe Mspm Rph Ccrp Rac’s Phone Numbers No phone number available.
Social Media
Msra Saurabh Kothari Msbe Mspm Rph Ccrp Rac’s Location Cambridge, Massachusetts, United States
Msra Saurabh Kothari Msbe Mspm Rph Ccrp Rac’s Expertise Master's level Regulatory professional with experience in domestic and international regulatory strategy and submissions, TMF Management, and Quality Assurance. International experience has also included Research and Pharmacovigilance. Ability to adapt to new environments and work with a wide variety of regulatory standards and guidelines.
Msra Saurabh Kothari Msbe Mspm Rph Ccrp Rac’s Current Industry Novo Nordisk
Msra
Saurabh Kothari Msbe Mspm Rph Ccrp Rac’s Prior Industry
Cnrs
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Novartis
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Timi Study
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Boston Scientific
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Takeda Pharmaceuticals
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Premier Research
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Ariad Pharmaceuticals
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Evelo Biosciences
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Uc San Diego Extension
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Northeastern University
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Novo Nordisk
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Work Experience

Novo Nordisk
Global Regulatory Lead
Tue Aug 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Northeastern University
Adjunct Faculty, MS Regulatory Affairs Program
Sat Jan 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Uc San Diego Extension
Adjunct Faculty, Quality Assurance
Tue Jun 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Evelo Biosciences
Director of Regulatory Affairs
Mon Jul 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon May 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time)
Evelo Biosciences
Regulatory Affairs Manager
Wed Nov 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Jul 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time)
Ariad Pharmaceuticals
Regulatory Affairs Senior Strategy Associate
Tue Nov 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Nov 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time)
Premier Research
Clinical Trial Associate
Sat Oct 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Nov 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time)
Takeda Pharmaceuticals
Regulatory Affairs Associate
Sun May 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Jul 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time)
Boston Scientific
Quality Assurance Inspector II
Fri Jan 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Mar 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time)
Timi Study
Trial Master File Specialist
Wed Jul 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Nov 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time)
Timi Study
Regulatory Document Specialist/ Trial Master File Specialist
Thu Jan 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Nov 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time)
Novartis
Safety Processing Expert (intern)
Mon Jul 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Dec 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time)
Cnrs
Stem Cell Research - Developmental Neurobiology (Intern)
Tue May 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Jul 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time)