DaMar Staffing seeks an Associate Director of Medical Writing (Regulatory) to lead the development of regulatory documents across programs. Remote work is possible for candidates located in the United States, with West Coast hours required.
The role focuses on authoring CSRs, protocols, investigator brochures, and CTD summaries, while guiding cross-functional teams to ensure submission readiness. A strong background in FDA/EMA/ICH guidance and 10+ years of pharma/biotech writing is required.
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