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

JR United Kingdom; Hounslow; Remote; GBP 50,000 - 70,000; Full time

Job summary

A global clinical research organization is seeking a Senior Medical Writer to support the preparation of complex clinical documents. This home-based role in the UK offers an exciting opportunity to lead projects, author key documents for regulatory submissions, and mentor junior writers, contributing to the market introduction of vital therapies.

Qualifications

• Experience as a medical writer, especially with project leadership.
• Experience with Phase I - III protocol and CSR medical writing.

Responsibilities

• Author high-complexity study-level documents including protocols and investigator brochures.
• Guide junior medical writers and lead multiple projects.

Skills

Project management

Stakeholder management

Job description

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Senior Medical Writer - 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:

1

Posted:

04.06.2025

Expiry Date:

19.07.2025

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

As a 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 independently author:

• Clinical evaluation plans and Clinical evaluation 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 significant role in bringing key therapies to market across various therapeutic areas. You will be assigned to one sponsor, lead multiple projects, and supervise and guide junior medical writers.

For this position, our client is seeking someone with experience as a medical writer, especially with project leadership on medical writing projects.

You should also have experience with:

• Phase I - III protocol and CSR medical writing
• Stakeholder management - internal and external
• Project management and leadership skills

For more information on this position 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.