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

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

Job summary

A leading global Clinical Research Organisation is seeking a Medical Writer II to author key clinical documents and manage projects. This home-based role in the UK presents an opportunity to significantly contribute to bringing crucial therapies to market across therapeutic areas, with responsibilities including stakeholder management and project leading.

Qualifications

• Experience as a medical writer.
• Experience working as project lead on medical writing projects.
• Phase I - III protocol and CSR medical writing experience.

Responsibilities

• Authoring study-level documents including protocols and ICFs.
• Interpreting and summarising data for clinical documents.
• Representing medical writing in relevant project groups.

Skills

Medical writing

Project management skills

Stakeholder management

Job description

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

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Client:

Planet Pharma

Location:

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

5

Posted:

06.06.2025

Expiry Date:

21.07.2025

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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) who is looking for an experienced Medical Writer to join the team and support with the preparation of submission and other complex clinical documents.

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

• Interpreting and summarising data
• Medical writing aspects of task finalisation including stakeholder alignment, coordination, and adherence to timelines.
• Representing medical writing in relevant project groups

This is an exciting opportunity to join a globally renowned CRO and play a big part in bringing key therapies to market across a variety of therapeutic areas. You will be assigned to one sponsor and you will get the chance to take project management responsibilities.

For this position, my client is looking for someone who has experience as a medical writer and has experience working as project lead on medical writing projects.

You will also have experience with:

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

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