Remote Regulatory Medical Writer – Oncology Trials

Cancer Research UK; City of Edinburgh; Hybrid; GBP 36,000 - 47,000; Full time

Job summary

A charitable organization focused on cancer research is seeking Regulatory Medical Writers for two contracts to support oncology trials. The role involves writing and reviewing clinical documents while ensuring compliance with regulatory standards. Ideal candidates will have medical writing experience and project management skills. Flexibility in work location is offered, along with a supportive environment and generous benefits.

Benefits

Generous benefits package

Opportunities for career development

Supportive work environment

Qualifications

• Significant experience in regulatory medical writing or a mix of regulatory and related clinical writing.
• Good knowledge of regulatory requirements for clinical trial documents.
• Experience within early-phase oncology trials is desirable but not essential.

Responsibilities

• Write, edit, and review clinical study reports and investigator brochures.
• Manage preparation of clinical study reports with project teams.
• Liaise with project team to complete project-specific tasks.

Skills

Proven experience in medical writing

Excellent proofreading skills

Confident communication skills

Project management skills

Education

Science graduate

Tools

AI medical writing tools

Job description

A charitable organization focused on cancer research is seeking Regulatory Medical Writers for two contracts to support oncology trials. The role involves writing and reviewing clinical documents while ensuring compliance with regulatory standards. Ideal candidates will have medical writing experience and project management skills. Flexibility in work location is offered, along with a supportive environment and generous benefits.