As a Senior Medical Writer, you will join the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.

You will support a Top-5 pharma company, helping 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. These include clinical study documents such as clinical summaries, protocols, CSRs, IBs, briefing books, response documents, and PIPs, covering phases from Phase 1 in patients to Phase 3 across multiple therapeutic areas.
• Analyze and critically interpret data to determine the best approach for each document, applying lean writing strategies.
• Act as the primary contact for the study team regarding the preparation and timelines (including planning) of assigned documents.
• Facilitate document review to ensure submission readiness and final approval. You will coordinate with QC personnel and publishing specialists supporting document preparation.

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• Minimum of a bachelor’s degree; Master’s degree preferred.
• 3-5 years of medical writing and relevant pharmaceutical experience, with strong scientific and regulatory knowledge.
• Strong writing skills with the ability to convert scientific data into clear, well-structured messages.
• Proficient in independently writing various clinical/regulatory documents (protocols, CSRs, etc.), including leading authoring, coordinating review, and ensuring documents are submission-ready and approved.