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

JR United Kingdom; City of Edinburgh; Remote; GBP 40,000 - 60,000; Full time

Job summary

A global clinical research organization is seeking a skilled Medical Writer II for a home-based role in Edinburgh. The successful candidate will author complex clinical documents and manage projects, playing a crucial role in the therapeutic development process. This position offers a unique opportunity to contribute significantly to impactful clinical trials and therapies.

Qualifications

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

Responsibilities

• Authoring study-level documents including protocols, ICFs, and investigator brochures.
• Interpreting and summarising data and ensuring stakeholder alignment.

Skills

Stakeholder management

Project management

Leadership skills

Job description

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

Planet Pharma is currently working with a global clinical research organisation (CRO) that is looking for an experienced Medical Writer to join the team and support the preparation of submission and other complex clinical documents.

As part of this role, you will be responsible for authoring most study-level documents including protocols, ICFs, lay summaries of clinical trial results, briefing packages, and investigator brochures. You will also be responsible for:

• Interpreting and summarising data
• Medical writing aspects of task finalisation 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 play a significant role in bringing key therapies to market across various therapeutic areas. You will be assigned to one sponsor and may take on project management responsibilities.

For this position, my 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 - internal and external
• Project management and leadership skills

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