Sandip Roy in

Sandip Roy

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Vice President, Head of Global Regulatory Affairs at Keenova
📍 Basking Ridge, New Jersey, United States

Sandip Roy is the Vice President and Head of Global Regulatory Affairs at Keenov, leveraging over two decades of experience in the biopharmaceutical industry. He holds a Ph. D. from the University of South Florida and has held senior leadership roles at Merck, Organon, and Mallinckrodt, specializing in global regulatory strategy.

He co-authored a clinical study on the pharmacokinetics of combining Amantadine and Oseltamivir, highlighting his deep expertise in drug interactions and pandemic influenza preparedness.

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Experience
22 Years
Current Role
Vice President, Head of Global Regulatory Affairs
Job Level
Senior
Location
Basking Ridge, New Jersey, United States
Personality Overview

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Priorities

Topics Sandip cares about

Global Regulatory Strategy
His entire career is focused on leading global regulatory affairs for major pharmaceutical companies like Merck, Organon, and Keenov.
Pharmaceutical Development
He has extensive experience across the drug development lifecycle, from clinical safety and pharmacovigilance to global product strategy.
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Career

Work history

11-2025
Vice President, Head of Global Regulatory Affairs
Keenova
10-2022 - 11-2025
Vice President, Global Head of Regulatory Affairs & Safety/ Pharmacovigilance
Mallinckrodt Pharmaceuticals
6-2021 - 10-2022
Head of US Regulatory Affairs & Global Product Strategy at Organon
Organon
10-2018 - 6-2021
Associate Vice President, Therapeutic Area Head of General Medicine, Global Regulatory Affairs
Merck
8-2015 - 10-2018
Executive Director, Global Regulatory Affairs & Clinical Safety, Vaccines and Inectious Disease
Merck
In the press

Media appearances

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Education
1994 - 1997
Fellowship
University of Chicago
1989 - 1993
Ph.D.
University of South Florida
Social presence
in
Behavioral profile

DISC profile (public)

DISC behavioral profile

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