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

JR United Kingdom; Chester; Remote; GBP 40,000 - 60,000; Full time

Job summary

A global clinical research organization is seeking a Medical Writer II to support submission preparation and complex clinical document authoring. The candidate will manage writing tasks and may take on project management responsibilities while contributing to the development of key therapies.

Qualifications

• Experienced Medical Writer with Phase I-III protocol writing.
• Background in project lead roles.
• Familiar with clinical document preparation.

Responsibilities

• Author study-level documents including protocols and investigator brochures.
• Manage medical writing tasks and coordinate with stakeholders.
• Represent medical writing in project groups.

Skills

Medical writing

Stakeholder management

Project management

Leadership skills

Job description

Medical Writer II - 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.

In this role, you will be responsible for authoring study-level documents including protocols, ICFs, lay summaries of clinical trial results, briefing packages, and investigator brochures. Your responsibilities will also include:

• Interpreting and summarising data
• Managing medical writing tasks, including stakeholder alignment, coordination, and adherence to timelines
• Representing medical writing in relevant project groups

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 and may take on project management responsibilities.

The ideal candidate will have experience as a medical writer, particularly working as a project lead on medical writing projects, including:

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

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