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Senior Medical Writer - Regulatory Submissions Lead

Integrated Resources Inc., Madison, NJ, United States


A leading staffing firm is seeking a Medical Author to document clinical data and regulatory submissions to support drug development. This role requires expertise in analytical writing, project management, and collaboration with product teams to ensure high-quality deliverables. Ideal candidates will possess a strong scientific background and experience in medical writing or pharmaceutical development. #J-18808-Ljbffr