Senior Medical Writing Leader
Prometrika
PROMETRIKA, a full-service CRO, seeks a Manager, Medical Writing to oversee the creation of regulatory documents for global drug development programs. The role includes writing and editing protocols, CSRs, and submissions, and supervising junior writers and contractors. The candidate should have at least 10 years in biotech/pharmaceuticals, 7+ years in regulatory writing, and experience with INDs, NDA/BLA/MAA submissions; CRO experience is strongly preferred. #J-18808-Ljbffr Prometrika
Vacancy posted 3 days ago
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