Kailera Therapeutics, Inc. in Massachusetts is seeking an Associate Director, Global Regulatory Affairs to lead day-to-day regulatory activities for early/late phase products, writing and submitting IND/CTA amendments and future marketing applications, and guiding teams on filings.
You will partner with Regulatory CMC and Regulatory Operations, provide regulatory intelligence, stay updated on global guidance, and respond to agency questions, with 10–15% travel.
#J-18808-LjbffrGlobal Regulatory Affairs Lead — IND/CTA Strategy in waltham at Unknown Company
This position is listed as full time and onsite.