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

JR United Kingdom; Leeds; Remote; GBP 45,000 - 70,000; Full time

Job summary

A leading global clinical research organization is seeking a Senior Medical Writer to support the preparation of critical clinical documents. The role requires authoring high-complexity study documents and managing projects, providing an exciting opportunity to contribute to key therapies on a global scale.

Qualifications

• Experience as a Medical Writer, especially in leading projects.
• Experience with Phase I - III protocol and CSR.
• Background in authoring complex clinical documents.

Responsibilities

• Author high complexity study-level documents including protocols and investigator brochures.
• Lead multiple projects and supervise junior writers.
• Manage internal and external stakeholders effectively.

Skills

Clinical evaluation plans

Stakeholder management

Project management

Job description

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Senior Medical Writer - Global Clinical Research Organisation - Home based in UK, leeds, west yorkshire

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Client:

Planet Pharma

Location:

leeds, west yorkshire, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

1

Posted:

06.06.2025

Expiry Date:

21.07.2025

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Job Description:

Senior Medical Writer - 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 Senior Medical Writer, you will be responsible for authoring high complexity study-level documents including protocols, ICFs, investigator brochures and meeting packages. You will also be responsible for independently authoring:

• Clinical evaluation plans and Clinical evaluations reports
• Paediatric Investigational Plans (PIPs)
• Clinical summary and overview documents in CTD/eCTD formats for global regulatory submissions

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 be leading on multiple projects, as well as supervising and providing guidance to more junior medical writers.

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.