Senior Medical Writer - Remote Regulatory Documents Lead
PAREXEL
Parexel is seeking a Medical Writer in the United States to author and revise clinical documents for regulatory submissions. The role requires strong writing/editing skills, adherence to regulatory guidelines, and collaboration with cross-functional teams on project timelines. Expertise in protocol development, reports, and CTD overviews is essential. The position emphasizes SOP compliance, literature reviews, and delivering high-quality content while supporting client needs and project #J-18808-Ljbffr
Vacancy posted 3 days ago
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