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

JR United Kingdom; Bournemouth; Remote; GBP 45,000 - 65,000; Full time

Job summary

A global clinical research organisation is seeking a Senior Medical Writer for a home-based role in Bournemouth. This position involves authoring complex clinical documents and leading projects while supervising junior writers. Ideal candidates should have significant experience in medical writing and project management.

Qualifications

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

Responsibilities

• Authoring high-complexity study-level documents including protocols and investigator brochures.
• Guiding junior medical writers and leading multiple projects.

Skills

Stakeholder management

Project management

Leadership skills

Job description

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

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 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 contribute to bringing key therapies to market across various therapeutic areas. You will be assigned to one sponsor, leading multiple projects, and supervising and guiding junior medical writers.

For this position, the client is looking for 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 experience
• Stakeholder management, both internal and external
• Project management and leadership skills

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