Job description
**Position Title: CMC Program Manager**
Lead comprehensive CMC program management for advanced mid to late-stage initiatives, encompassing the creation of timelines, evaluation of risks, and monitoring of execution. Facilitate the preparation and submission of CMC elements for international regulatory applications while fostering collaboration with cross-functional teams. This role necessitates a Ph.D. or M.S. in a pertinent scientific field and a minimum of 10 to 15 years of experience in CMC. Ideal candidates will possess demonstrated proficiency in managing oral small molecule programs, overseeing CDMO/CRO relationships, and navigating global regulatory standards.
Kymera Therapeutics provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
