Senior Medical Writer
Bristol Myers Squibb EU Policy
Bristol Myers Squibb is seeking a Senior Scientific Writer I to develop and manage regulatory documentation for clinical submissions, including CSR and CTD sections. The role requires strong collaboration with cross-functional teams to ensure alignment with global regulatory standards. You will maintain high-quality, consistent documents across text, tables, and figures, and mentor a diverse group of authors while driving timelines and quality. #J-18808-Ljbffr
Vacancy posted 4 days ago
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