Ecrivain Public jobs in France

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You will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence.

Supporting a Top-5 pharma company, you will help deliver best-in-class regulatory and submission documents. While employed with ICON, you will be fully embedded with our client.

• Independently produce clinical and regulatory documents in collaboration with Principal Medical Writers, including Clinical Study Protocols and Clinical Study Reports across Phase 1 to Phase 3 in multiple therapeutic areas.
• Analyze and interpret data critically to determine the best approach for each document, applying lean writing strategies.
• Act as the primary contact for the study team regarding document preparation and timelines, including planning.
• Facilitate document review, ensuring documents are submission-ready and approved, working directly with QC personnel and publishing specialists.

• Bachelor’s degree required; Master’s degree preferred.
• 3-5 years of Medical Writing or relevant pharmaceutical experience with scientific and regulatory knowledge.
• Strong writing skills with the ability to convert scientific data into clear, well-structured messages.
• Proficiency in independently writing clinical/regulatory documents (mainly CSRs, Protocols), leading creation, coordination, review facilitation, and ensuring submission readiness.