Todas as vagas
Principal Medical Writer
ICON plc
Frankfurt +4 · Aceita remotoSênior (5–10 anos)Tempo integralPublicada em 21 de ago. de 2026
Sobre a vaga
O que você vai fazer
Lead the development of high-quality regulatory and clinical documents to support submissions to global regulatory authorities. Manage medical writing projects, including timeline development and cross-functional coordination to ensure compliance with industry standards.
O que eles procuram
Requires a Bachelor's degree in life sciences and at least 6 years of medical writing experience within the biopharmaceutical or CRO industry. Must be proficient in regulatory writing for Clinical Study Reports and Protocols, with oncology experience preferred.
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