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

JR United Kingdom; Hounslow; Remote; GBP 40,000 - 65,000; Full time

Job summary

A global clinical research organization is looking for a Medical Writer II to prepare complex clinical documents, manage projects, and collaborate with stakeholders. This home-based position in South West London offers the chance to work on significant therapies across various therapeutic areas.

Qualifications

• Experience in medical writing, particularly in project lead roles.
• Phase I-III protocol and CSR medical writing experience.

Responsibilities

• Author study-level documents including protocols, ICFs, and investigator brochures.
• Interpret and summarize data, handle stakeholder alignment.

Skills

Stakeholder management

Project management

Job description

Social network you want to login/join with:

Medical Writer II - Global Clinical Research Organisation - Home based in UK, south west london

Client: Planet Pharma

Location: south west london, 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) that is looking for an experienced Medical Writer to join the team and support the preparation of submission and other complex clinical documents.

In this role, you will be responsible for authoring study-level documents including protocols, ICFs, lay summaries of clinical trial results, briefing packages, and investigator brochures. You will also:

• Interpret and summarize data
• Handle medical writing tasks, including stakeholder alignment, coordination, and adherence to timelines
• Represent medical writing in relevant project groups

This is an exciting opportunity to join a globally renowned CRO and contribute to bringing key therapies to market across various therapeutic areas. You will be assigned to one sponsor and may take on project management responsibilities.

The ideal candidate will have experience as a medical writer, particularly working as a project lead on medical writing projects, with:

• Phase I - III protocol and CSR medical writing experience
• Stakeholder management skills (internal and external)
• Project management/project lead skills

For more information or similar opportunities, please contact Chanel Hicken at 0203 868 1011 or email your updated CV to [emailprotected]. We can arrange a confidential discussion on how you can get involved in this exciting opportunity.