DaMar Staffing seeks an Associate Director of Medical Writing (Regulatory) to lead the creation of high‑quality regulatory documents across programs. This senior role guides CTD summaries, CSRs, protocols, and briefing packages, partnering with cross‑functional teams and ensuring submission readiness.
The ideal candidate has 10+ years in medical writing within pharma/biotech, strong leadership, and a solid grasp of FDA/ICH guidelines.
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