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Job description
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.
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Worksite address
waltham, MA, 02254, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.