Associate Director, Medical Writing — Regulatory Lead
Structure Therapeutics
Location: South San Francisco, California, United StatesCompany: Structure TherapeuticsPosted: 2026-10-03Structure Therapeutics is seeking an Associate Director of Medical Writing to lead the development of regulatory and clinical documents for its drug programs. The role requires expertise in regulatory writing, QC, and cross‑functional collaboration to ensure compliant, timely submissions.You will manage multiple projects, mentor writers, and align messaging across documents while partnering with Clinical Sciences, Regulatory Affairs, Biostatistics, and other teams.#J-18808-Ljbffr
$230k - $240k
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...and capitalizing on the strengths of each geographic location.Position Summary:The Associate Director of Medical Writing will be responsible for leading the development of key regulatory and clinical documents supporting the company’s drug development programs, while also...MedicalRegulatoryContract workRemote work- 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...MedicalRegulatoryRemote job
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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. Responsibilities authoring, reviewing, and finalizing...MedicalRegulatoryRemote work- Structure Therapeutics Inc. is seeking an Associate Director of Medical Writing to lead regulatory and clinical document development, ensure quality and compliance, and coordinate cross-functional inputs across Clinical Sciences, Regulatory Affairs, Biostatistics, and...MedicalRegulatory
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..., supporting exploratory analyses, early regulatory engagements, and complex data-generation... ...interactive dashboards that drive high-quality Medical Data Review (MDR) and safety signal... ...with the evolving development strategy. You lead the statistical design of complex or high...MedicalRegulatoryFull timeLocal areaRelocation package- Zai Lab Limited is seeking an Associate Director, Regulatory Affairs to lead regulatory strategy and execution for global programs. This remote role... ...collaborates with Clinical, Nonclinical, Biometrics, Medical Writing, CMC, and other teams to ensure timely submissions...MedicalRegulatoryRemote job
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