Senior Regulatory Medical Writer CSR/CTD Specialist
Bristol-Myers Squibb
Bristol Myers Squibb is looking for a Senior Scientific Writer I to author complex clinical documents and participate in document strategy and prototyping sessions. This role requires leadership in influencing authors from diverse disciplines, ensuring high-quality regulatory submissions. The ideal candidate will manage timelines, maintain documentation standards, and innovate in medical writing while adhering to regulatory guidelines. #J-18808-Ljbffr
Vacancy posted 5 hours ago
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