Associate Director, Regulatory CMC — Global Submissions & Strategy

Job description

Summit Therapeutics, Inc. is seeking an experienced Associate Director of Regulatory Affairs, CMC to coordinate global regulatory filings. This role requires a Bachelor's degree in Chemistry or related field, at least 6 years of Regulatory CMC experience, and thorough knowledge of FDA and EU regulations. The position focuses on managing CMC regulatory aspects and preparing submissions. The salary range for this position is approximately $194,000 - $199,000 USD per year, based on experience and skills. Hybrid work-model applies, with office presence in California.

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Worksite address

palo alto, CA, 94306, US

Who can apply

Review the original listing for work authorization, qualifications and employer requirements.