Dyne Therapeutics

Medical Director

• Provide strategic leadership and hands-on execution for high-quality, compliant clinical and regulatory documents supporting development programs
• Partner with Clinical Development, Clinical Operations, Clinical Pharmacology, Regulatory Affairs, Research, Preclinical, Translational Biomarkers, Program Management, and Medical Affairs
• Lead planning, authoring, review, and completion of documents for FDA and global health authority submissions
• Manage internal and external medical writing resources to deliver accurate, high-quality documents on time
• Author, edit, and collaborate on protocols, investigator brochures, clinical study reports, CTD modules, briefing books, and related submission materials
• Review and refine contributor-prepared documents for quality, consistency, scientific accuracy, and regulatory adherence
• Contribute to project planning and cross-functional working groups
• Establish and improve medical writing processes, templates, and best practices

Explore Director, Medical Writing at Dyne Therapeutics. Review requirements and application details.

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Director, Medical Writing