Senior Clinical Regulatory Writer
Há 4 dias
Coimbra, Portugal
Med Communications International
Tempo integral
60 000 € - 90 000 € Contrato
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Med Communications International in Europe is seeking a Regulatory Writing Specialist with at least 3 years of hands-on pharmaceutical regulatory writing experience, including clinical study reports, protocols, IBs, and CTD Module 2 documents. The role focuses on authoring, QC, and coordinating client-facing regulatory deliverables for submissions (IND/NDA/BLA/MAA).
You will work remotely across Europe, liaise with cross-functional teams, and ensure quality and timely delivery of regulatory