Todas as vagas
Senior Medical Writer
Holanda · Aceita remotoSênior (5–10 anos)Tempo integralPublicada em 17 de ago. de 2026
Sobre a vaga
O que você vai fazer
The Senior Medical Writer is responsible for preparing critical regulatory documents including IND applications, clinical study protocols, and investigator's brochures for oncology trials. The role involves collaborating directly with clients, medical monitors, and senior leadership to manage document timelines and review cycles.
O que eles procuram
Candidates must have a bachelor's degree and over 5 years of experience in a CRO or pharmaceutical environment, with at least 3 years specifically in oncology regulatory medical writing. Proven experience as a lead writer for major regulatory documents and familiarity with eCTD modules and international regulatory guidelines are required.
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