Medical Writer

4 weeks ago

London, United Kingdom Hays Full time

My client has a position available for a Regulatory /Clinical Medical Writer to join their team for a 6-month initial contract within their rare diseases arena.
Hybrid, London – 2–3 days WFH

As the Regulatory/ Clinical Medical Writer, you will be involved in the authoring of regulatory and clinical documents such as protocols, core dossiers, CSRs, briefing books, responses to questions. QC and light project management (managing timelines), chairing adjudication meetings. You will be an experienced medical writer at developing complex clinical and regulatory documents within the rare disease landscape.

Medical writer in the pharmaceutical industry
 Medical or scientific writing experience as a primary job responsibility

In order to apply for the Medical Writer contract, you must possess:
• Bachelor's degree in a scientific discipline
• Demonstrated a clear, high-quality scientific writing style in the English language.
• Significant experience in writing regulatory and clinical documents such as protocols, core dossiers, CSRs, briefing books, responses to questions
• Great understanding of regulatory guidelines and stats
• Project management skills, consistently achieving multiple tasks and goals on-time.
• Able to work with minimal supervision and support.
• Before you apply for this position, it is vital that you are in possession of a UK passport or relevant visa to work without restrictions in the UK and must be based in the UK.

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