Medical Writer II - Global Clinical Research Organisation - Home based in UK

JR United Kingdom; Reading; Remote; GBP 40,000 - 60,000; Full time

Job summary

Join a leading global clinical research organisation as a Medical Writer II, where you will author critical clinical documents and manage writing tasks. This home-based position in Reading offers a unique opportunity to contribute to the development of therapies and gain invaluable project management experience. Ideal candidates will have previous medical writing experience with a proven track record in protocol development and stakeholder engagement.

Qualifications

• Experience as a medical writer with Phase I - III protocol and CSR experience.
• Stakeholder management skills required.
• Project management or lead experience preferred.

Responsibilities

• Authoring study-level documents including protocols and investigator brochures.
• Interpreting and summarising clinical data.
• Managing medical writing tasks and project timelines.

Skills

Stakeholder management

Project management

Job description

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Medical Writer II - Global Clinical Research Organisation - Home based in UK, Reading

Client: Planet Pharma

Location: Reading, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views:

2

Posted:

04.06.2025

Expiry Date:

19.07.2025

Job Description:

Medical Writer II - Global Clinical Research Organisation - Home based in UK

Planet Pharma is currently working with a global clinical research organisation (CRO) seeking an experienced Medical Writer to support the preparation of submission and other complex clinical documents.

Responsibilities include:

• Authoring study-level documents such as protocols, ICFs, lay summaries, briefing packages, and investigator brochures
• Interpreting and summarising data
• Managing medical writing tasks, stakeholder alignment, coordination, and adhering to timelines
• Representing medical writing in project groups

This role offers the opportunity to join a renowned CRO and contribute to bringing therapies to market across various therapeutic areas. You will be assigned to a sponsor and may take on project management responsibilities.

Requirements include:

• Experience as a medical writer with Phase I - III protocol and CSR experience
• Stakeholder management skills
• Project management or lead experience

For more information or to apply, contact Chanel Hicken at 0203 868 1011 or email your CV to [emailprotected]. We look forward to discussing this exciting opportunity with you.