Associate Director, Medical Writing

Rapport Therapeutics · Boston, MA

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Role summary

Rapport Therapeutics seeks an Associate Director of Medical Writing to lead clinical and regulatory documentation for its RAP-219 neuromedicine portfolio. The role involves developing protocols, study reports, and regulatory submissions while integrating AI-enabled tools and collaborating across functions to support program advancement.

What they're looking for

Extensive experience in clinical and regulatory medical writing
Demonstrated expertise in AI-enabled tools and emerging technologies
Strong knowledge of regulatory guidelines and medical writing standards
Proven ability to manage cross-functional stakeholder collaboration
Experience developing clinical protocols and regulatory submissions
Track record of implementing process improvements and automation solutions

What you'll be doing

Lead writing and review of clinical protocols, study reports, and regulatory documents for RAP-219 program
Collaborate across medical, clinical, regulatory, and biostatistics teams to ensure document accuracy and alignment
Evaluate and implement AI tools and automation to improve document development and workflow efficiency
Provide strategic guidance on document structure, content, and timelines for health authority submissions
Contribute to modernization of medical writing processes, templates, and standards

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Date posted2 days ago

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