Saurabh Kothari Email & Phone Number
Global Regulatory Lead @ Novo Nordisk
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Saurabh Kothari Location
- Boston, MA, US
Saurabh Kothari Work
- 2023 -now Global Regulatory Lead @
- 2025 -now Adjunct Faculty, MS Regulatory Science Program @
- 2021 -now Adjunct Faculty, Quality Assurance and Regulatory Affairs Certificate Program @
- 2022 -2026 Adjunct Faculty, MS Regulatory Affairs Program @
- 2019 -2023 Director of Regulatory Affairs @
- 2017 -2019 Regulatory Affairs Manager @
- 2016 -2017 Regulatory Affairs Senior Strategy Associate @ ARIAD Pharmaceuticals, Inc.
- 2016 -2016 Clinical Trial Associate @
- 2016 -2016 Regulatory Affairs Associate @
- 2016 -2016 Quality Assurance Inspector II @
- 2015 -2015 Trial Master File Specialist @
- 2015 -2015 Regulatory Document Specialist and Trial Master File Specialist @
- 2013 -2013 Safety Processing Expert (intern) @
- 2012 -2012 Stem Cell Research - Developmental Neurobiology (Intern) @
Saurabh Kothari Education
- Questrom School of Business, Boston University
Master of Business Administration - MBA
2025-2027 - Harrisburg University of Science and Technology
Master of Science (MS) (Project Management)
2017-2019 - Northeastern University
Master of Science (MS) (Regulatory Affairs for Drugs, Biologics, and Medical Devices)
2014-2016 - Birla Institute of Technology and Science, Pilani
Master of Science (MS) (Biomedical/Medical Engineering)
2008-2013 - Birla Institute of Technology and Science, Pilani
Bachelor’s Degree (Pharmacy)
2008-2013
Saurabh Kothari Skills
- Oberon
- Clinical Trials
- Archives
- Technical Reviews
- Outline
- Matlab
- Students
- Clinical Research
- CTMS
- Biotechnology
- Regulatory Affairs
- Career Development
- Proliferation
- Tracker
- SAP ERP
- Quality Auditing
- Paperwork
- MHRA
- Regulatory Compliance
- Canadian
- Cda
- HTTPS
- Management
- Design
- Pediatrics
- Science
- Sop
- Metrics
- Death
- Pegasus
- Auditing
- Stem Cell Research
- PowerPoint
- Monitors
- Boston
- STEM
- SharePoint
- Approvals
- Human Resources
- Drug Product
- HPLC
- Pharmaceutical Research
- GMP
- Neurons
- Regulatory Documentation
- System
- Cell
- Differentiation
- Sage Act
- Reports
- Learning Management Systems
- Medicine
- Risk Management
- Microsoft Excel
- GCP
- Reporting Tool
- Retina
- Regulatory Submissions
- Documentation
- Quality Control
- Research
- Investigation
- EMA
- CAPA
- Multi Unit
- Inspection
- Combination
- Hospitals
- Medical Research
- Raps
- Sterilization
- Project Estimation
- SAP
- Eu Risk Management Plan
- C
- Coordination
- FIX Protocol
- Women's
- Query Writing
- GDP
- Life Sciences
- Quality Assurance
- Scientific
- MedDRA
- Novartis
- Safety
- Argus
- Checks
- Project
- France
- Drug Safety
- Pharmacy
- Hyderabad
- CTA
- Responsibility
- Pathway
- Rems
- Regulations
- Labelling
- Rmp
- Biology
- Paris
- History
- Microsoft Exchange
- IRB
- Reviews
- ICH guidelines
- Academic
- Guidelines
- Confidential Documents
- Bridge Inspection
- Medical Devices
- Software
- Compliance
- Biological Sciences
- Equities
- Pharmacovigilance
- Dissolution
- Microsoft Word
- Canada
- India
- Pharmaceutics
- Stability
- Tablets
- Pharmacoeconomics
- Formulation
- Regulatory Development
- Pharmaceutical Industry
- Delivery
- Analytical Method Validation
- FDA
- Coordinate
- Gaps
- Signalling
- Databases
- u.s. Food and Drug Administration
- Corrective and Preventive Action
- Good Clinical Practice
- Standard Operating Procedure
Saurabh Kothari Summary
- Saurabh Kothari, based in Boston, MA, US, is currently a Global Regulatory Lead at Novo Nordisk. Saurabh Kothari brings experience from previous roles at The Johns Hopkins University, UC San Diego Extension, Northeastern University and Evelo Biosciences. Saurabh Kothari holds a 2025 - 2027 Master of Business Administration - MBA @ Questrom School of Business, Boston University. With a robust skill set that includes Oberon, Clinical Trials, Archives, Technical Reviews, Outline and more. Saurabh Kothari has 2 emails and 1 mobile phone numbers on RocketReach.
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