Tyler Butt in

Tyler Butt

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Senior Director, Regulatory Affairs at Pfizer
📍 New York, New York, United States

Tyler is the Senior Director of Regulatory Affairs at Pfizer, where he leads U. S. FDA strategy for late-stage and marketed pharmaceuticals. With a Master of Science from Columbia University, he specializes in NDA submissions and post-market lifecycle management, focusing on mitigating risk and ensuring regulatory clarity for complex therapies.

He has a keen interest in how the Regulatory Affairs function is evolving from a downstream role to being central to innovation in the pharmaceutical industry.

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Current Role
Senior Director, Regulatory Affairs
Job Level
Senior
Location
New York, New York, United States
Personality Overview

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Priorities

Topics Tyler cares about

U. S. FDA Strategy
He leads U. S. FDA regulatory strategy for late-stage and marketed pharmaceutical products, serving as the primary liaison for meetings and submissions.
Drug Development
His focus is on late-stage drug development, overseeing NDA and sNDA submissions, and managing post-approval lifecycle updates.
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Career

Work history

Senior Director, Regulatory Affairs
Pfizer
Associate Director, Regulatory Affairs
Bristol Myers Squibb
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Education
Master of Science (MS)
Columbia University
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Behavioral profile

DISC profile (public)

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