Kailera Therapeutics seeks an Associate Director, Global Regulatory Affairs to lead day-to-day regulatory activities for early and late-phase investigational products, guiding IND/CTA submissions and future marketing applications, and advising cross-functional teams on regulatory filings.
The role collaborates with Regulatory CMC and Regulatory Operations to ensure scientific data and submissions meet agency expectations in a compliant manner. Onsite in Waltham, MA, 3–4 days a week.
#J-18808-LjbffrGlobal Regulatory Affairs Lead - IND/CTA Submissions in boston at Unknown Company
This position is listed as full time and onsite.