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

JR United Kingdom; Reading; Remote; GBP 45,000 - 75,000; Full time

Job summary

A leading global clinical research organisation seeks an experienced Senior Medical Writer to contribute to the preparation of complex clinical documents. The ideal candidate will possess significant experience in medical writing, project management, and stakeholder engagement while leading projects and supporting junior writers.

Qualifications

• Experience as a medical writer and project lead.
• Specific experience in Phase I - III protocol and CSR medical writing.
• Strong project management and stakeholder management skills.

Responsibilities

• Author high-complexity study-level documents including protocols and investigator brochures.
• Supervise or guide junior medical writers.
• Lead multiple projects for a single sponsor.

Skills

Stakeholder management

Project management

Leadership skills

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. You will also independently author:

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

This is an exciting opportunity to join a globally renowned CRO and contribute to bringing key therapies to market across various therapeutic areas. You will be assigned to one sponsor, lead multiple projects, and supervise or guide junior medical writers.

The ideal candidate will have experience as a medical writer and project lead on medical writing projects, with specific experience in:

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

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