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

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

Job summary

A global clinical research organization is seeking a Medical Writer II for a home-based position in the UK. The role involves authoring critical clinical documents, managing projects, and engaging with various stakeholders. Ideal candidates will have a proven track record in medical writing and project leadership, contributing significantly to the development of key therapies.

Qualifications

• Experience as a medical writer with project lead skills.
• Experience with Phase I - III protocol and CSR medical writing.
• Proficient in managing stakeholders both internally and externally.

Responsibilities

• Author study-level documents including protocols and briefing packages.
• Interpret and summarize data for medical writing.
• Coordinate task finalization with stakeholders.

Skills

Medical writing

Stakeholder management

Project management

Data interpretation

Job description

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Medical Writer II - Global Clinical Research Organisation - Home based in UK, kingston upon hull, east yorkshire

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Client:

Planet Pharma

Location:

kingston upon hull, east yorkshire, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

2

Posted:

04.06.2025

Expiry Date:

19.07.2025

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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.