Kailera Therapeutics is seeking an Associate Director, Global Regulatory Affairs to lead day-to-day regulatory activities for early and late-stage investigational products, guiding IND/CTA submissions and future marketing applications. You will partner with Regulatory CMC and Operations to align data with agency expectations.
Required location: Waltham, MA, hub-based onsite 3-4 days/week. A Bachelor’s with 10+ years or an Advanced degree with 5+ years in drug development is required.
#J-18808-LjbffrGlobal Regulatory Affairs Lead, Associate Director in waltham at Unknown Company
This position is listed as full time and onsite.