Regulatory Medical Writer Ii
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Fortrea is seeking a Regulatory Medical Writer II to own high-complexity clinical regulatory documents across Phase II-IV. You will manage the full document lifecycle, from planning and stakeholder engagement through drafting, review and final delivery, collaborating with cross-functional teams globally. The role requires 3 years of regulatory medical writing experience, at least 1 year leading MW projects, and strong knowledge of ICH guidelines.
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Principal Medical Writer
Há 6 horas
Moscavide E Portela, Portuguese Republic, Portugal Syneos Health Tempo integralMedical writer needed to create regulatory submission documents, ensuring scientific accuracy and managing project activities. Requires experience in biopharmaceutical industry.