Medical Writer – Future roles (UK)

Overview

In this role you will create and coordinate clinical and regulatory writing deliverables to present scientific information clearly. You will work with cross-functional teams, ensuring outputs meet regulatory and client standards on time and within budget. The role supports multiple documents from protocols to study reports, while maintaining quality and compliance. This position offers the chance to impact how data is communicated to stakeholders and to grow within a collaborative, globally minded organization.

Pay / Benefits

• career development and progression
• supportive and engaged line management
• technical and therapeutic area training
• peer recognition
• total rewards program

Responsibilities

• Compile, write, edit, and coordinate medical writing deliverables across departments under moderate supervision
• Produce documents such as clinical study protocols, protocol amendments, clinical study reports, patient narratives, and investigator brochures
• Adhere to ICH E3 guidelines, SOPs, templates, authorship and style guides; ensure on-time, on-budget delivery
• Coordinate quality and editorial reviews; lead document reviews and resolve client comments
• Review SAPs and table/figure/listing specs for content, grammar, and formatting
• Engage with clients and internal stakeholders to produce high-quality deliverables
• Conduct online literature searches and ensure copyright compliance
• Identify and propose solutions for document issues; escalate when needed
• Continue professional development to stay current with industry standards
• Monitor budgeted hours and communicate status; complete administrative tasks on time
• Occasional travel (<25%)
• Remain adaptable as responsibilities may evolve

Key requirements

• Familiarity with ICH E3 guidelines
• Experience in medical writing deliverables (protocols, CSRs, patient narratives, brochures)
• Ability to coordinate reviews and manage client feedback
• Understanding of statistical analysis plans and table/figure specifications
• Strong client and cross-functional collaboration skills
• Budget awareness and time management skills
• Good communication and organizational abilities
• Knowledge of copyright requirements and literature search basics
• Proactive issue identification and problem-solving mindset
• Commitment to ongoing professional development

• collaborative
• client-focused
• communication
• medical writing
• clinical study protocols
• clinical study reports

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