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

JR United Kingdom; Wolverhampton; 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 vital clinical documents in Wolverhampton. This role demands expertise in medical writing and project management, offering the chance to lead crucial projects and guide junior writers in a home-based setting.

Qualifications

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

Responsibilities

• Author high-complexity study-level documents including protocols and investigator brochures.
• Lead multiple projects, supervising junior medical writers.

Skills

Stakeholder management

Project management

Leadership skills

Job description

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

Client: Planet Pharma

Location: Wolverhampton, UK

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 their 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. Additionally, you will 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 and lead multiple projects, supervising and providing guidance to junior medical writers.

For this position, the client is seeking someone with experience as a medical writer and project lead on medical writing projects.

You should also have experience with:

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

For more information or similar opportunities, please contact Chanel Hicken at 0203 868 1011 or email your updated CV to [emailprotected] to arrange a confidential discussion about this exciting opportunity.