Rapport Therapeutics in Boston is seeking an experienced, AI-forward Associate Director, Medical Writing to lead clinical and regulatory documentation for the RAP-219 program. You will plan, develop, and deliver high-quality manuscripts and regulatory submissions.
The role requires 8+ years in medical writing, leadership on late-phase programs, and strong knowledge of ICH, FDA, EMA guidelines; you will evaluate AI tools to improve efficiency while safeguarding data integrity.
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