Global Regulatory Affairs Director, Submissions & Strategy
kailera therapeuticsNorthern, KY
Global Regulatory Affairs Director, Submissions & Strategy
kailera therapeuticsNorthern, KY
today
Industries
Pharmaceutical Preparation ManufacturingBiological Product (except Diagnostic) ManufacturingResearch and Development in Biotechnology (except Nanobiotechnology)About the role
Kailera Therapeutics, Inc. is seeking an Associate Director of Global Regulatory Affairs to lead day-to-day regulatory activities for investigational products and future marketing submissions. You will guide teams on IND/CTA filings, provide regulatory intelligence, and ensure compliance across global development programs. The role requires deep regulatory expertise, cross-functional collaboration, and willingness to travel (10–15%).
Matching similar jobs
JOB OVERVIEW
Experience level
Manager
Location
Northern, KY
Occupation
Regulatory Affairs Managers
Industry
Pharmaceutical Preparation Manufacturing
Posted
today
Tired of running searches?
Rank the roles you'd take once, and matches like these arrive on their own.
CREATE PROFILE