BIO
Ryan Zettle
Senior Director, Head of Regulatory Submissions, Americas, Regulatory Consulting
At Parexel, Ryan leads U.S. regulatory submissions team, supporting drug development and providing guidance to clients. He serves as client liaison and main point of contact to ensure that deliverables meet quality standards and communication aids in project success. He is responsible for leading major submissions within the U.S. including investigational new drug (IND) applications, new drug applications (NDAs), and post-approval.
Work Experience
An expert in regulatory affairs, Ryan joined Parexel in 2018 from the FDA, where he served as regulatory business project manager.
His prior experience also includes tenure as a clinical pharmacist with the Winslow Indian Health Care Center in Arizona.
Education
Ryan earned his Doctor of Pharmacy from Ohio Northern University in Ada, OH in 2011, followed by a Master of Business Administration from Trident University in Cypress, CA in 2019.