About the role

Kailera Therapeutics, Inc. in the United States seeks an Associate Director, Global Regulatory Labeling and Ad Promo to lead labeling activities and ensure regulatory compliance across product lifecycle. You will partner with clinical, CMC, medical, safety, and commercial teams to align labeling with available data and regulatory requirements. This role requires advanced degree with 5+ years in drug development or a bachelor’s with 10+ years.

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JOB OVERVIEW

Experience level

Lead

Location

Waltham, MA

Occupation

Regulatory Affairs Managers

Industry

Pharmaceutical Preparation Manufacturing

Posted

yesterday

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