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Senior Medical Writer & Regulatory Lead

ProPharma

ProPharma is seeking a senior medical writer to oversee the creation of regulatory and clinical documents across drugs, biologics, and medical devices. The role requires leading medical writing teams, coordinating with clinical operations, data management, and regulatory affairs to ensure timely, compliant submissions. The candidate will author and edit high-quality reports, CSRs, protocols, and PI summaries, while mentoring junior writers and maintaining industry-standard documentation #J-18808-Ljbffr

Vacancy posted 5 days ago
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