Medical Writer

Medical Writer – Oncology – Central London

We’re looking for an experienced Medical Writer to join a growing drug development company based in central London, focused on advancing innovative oncology treatments.

This is an exciting opportunity to be part of a small, agile, and collaborative team working across five oncology assets in pre-clinical and early-phase development. You’ll work closely with cross-functional experts, reporting to the Senior Clinical Scientist, to create, review, and edit high-quality regulatory and scientific documentation that supports the company’s development pipeline.

Key Responsibilities:

• Develop and review early-stage clinical study protocols and amendments

• Prepare Investigator Brochures

• Conduct literature reviews to source reference materials and understand the competitive landscape
• Author components of regulatory submissions and responses (e.g. INDs, DSURs, briefing documents, etc.)

• A degree in Life Sciences or a related field; an MSc or PhD is preferred
• Experience in oncology, ideally across multiple modalities
• Proven experience as a Medical Writer or Clinical Scientist, with the confidence and ability to work independently and proactively across the organisation
• Strong experience writing study protocols, amendments, and ancillary regulatory documents for Phase I and II oncology trials

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