Associate Director, Medical Writing

Role: Associate Director, Medical Writing at Rapport Therapeutics, responsible for leading clinical and regulatory document development within the RAP-219 neuromedicines program. Core responsibilities include preparing and reviewing clinical study protocols, reports, Investigator’s Brochures, and regulatory submissions; collaborating across functions such as medical science, clinical operations, and regulatory teams; providing strategic guidance on document content and timelines; and evaluating AI-enabled tools to enhance efficiency and quality. The role emphasizes staying current with regulatory standards (ICH, FDA, EMA) and advancing the integration of digital technologies in medical writing. Requirements: 8+ years of industry experience in medical writing, proven leadership in late-phase (Phases 2-3) clinical program documentation, and a strong understanding of regulatory standards; an advanced degree in a scientific or health discipline is preferred. Experience with CNS therapeutic areas, familiarity with AI applications in document development, and stakeholder management skills are highly valued. The position reports directly to the Head of Medical Writing and involves a hybrid work setup in Boston, MA, with onsite presence Monday through Wednesday. The compensation range is approximately $185,000 to $205,000, complemented by comprehensive benefits and a collaborative, innovation-driven culture focused on gene-targeted neuromedicines and precision therapies.