Associate Director, Medical Writing - Bay Area

Role Associate Director of Medical Writing leading the development of regulatory and clinical documents for Structure Therapeutics' drug pipeline, primarily supporting cardiovascular, metabolic, and pulmonary indications. Responsibilitiesauthoring, reviewing, and finalizing documents such as Study Protocols, Study Reports, Investigator Brochures, and regulatory responses; ensuring compliance with FDA, EMA, ICH standards; conducting QC reviews for accuracy, formatting, and data integrity; managing multiple projects and cross-functional collaboration with Clinical Sciences, Regulatory Affairs, Biostatistics, and others; providing strategic guidance on document standards and best practices.