About the role

Structure Therapeutics seeks an Associate Director of Medical Writing to lead development of regulatory and clinical documents for its drug pipeline, supporting cardiovascular, metabolic, and pulmonary indications. This role partners with Clinical Sciences, Regulatory Affairs, Biostatistics, and others to ensure high-quality submissions. The position emphasizes compliance with FDA/EMA/ICH standards, document management best practices, and cross-functional leadership, with a remote-first setup

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JOB OVERVIEW

Experience level

Manager

Location

South San Francisco, CA

Occupation

Regulatory Affairs Managers

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

yesterday

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