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

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

Job summary

A global clinical research organization is seeking an experienced Medical Writer II to support the preparation of complex clinical documents. This role involves authoring study-level documents, managing projects, and stakeholder coordination, making it an exciting opportunity to contribute to bringing key therapies to market.

Qualifications

• Experience as a medical writer.
• Background in project lead roles for medical writing projects.

Responsibilities

• Authoring study-level documents including protocols and ICFs.
• Interpreting and summarising data for clinical documents.
• Coordinating finalisation of medical writing tasks with stakeholders.

Skills

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
• Finalising medical writing tasks with stakeholder alignment, coordination, and adherence to deadlines
• 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, with a background in working as a project lead on medical writing projects.

Required experience includes:

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

For more information or to discuss this opportunity further, please contact Chanel Hicken at 0203 868 1011 or email your updated CV to [emailprotected]. We look forward to arranging a confidential discussion about how you can get involved in this exciting role.