Medical Writer

CK Group- Science, Clinical and Technical; City Of London; On-site; GBP 45,000 - 65,000; Full time

Job summary

A growing drug development company in central London is seeking an experienced Medical Writer specializing in oncology. You will develop and review clinical study protocols, prepare investigator brochures, and author regulatory submissions. Ideal candidates should possess a degree in Life Sciences, experience in oncology, and a strong background in medical writing. This role offers a collaborative environment focused on advancing innovative treatments.

Qualifications

• 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.

Responsibilities

• Develop and review early-stage clinical study protocols and amendments.
• Prepare Investigator Brochures.
• Conduct literature reviews to source reference materials.
• Author components of regulatory submissions and responses.

Skills

Medical Writing in Oncology

Regulatory Submissions

Literature Reviews

Study Protocol Development

Education

Degree in Life Sciences

MSc or PhD in relevant field

Job description

Overview

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.

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.)

Qualifications

• 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