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

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

Job summary

A global clinical research organization seeks an experienced Medical Writer II to join their home-based team in Bournemouth. This role involves authoring clinical documents, managing stakeholders, and overseeing project timelines. Ideal candidates will have a strong background in medical writing and project management, with skills in Phase I - III protocol writing and stakeholder relations.

Qualifications

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

Responsibilities

• Authoring study-level documents including protocols and ICFs.
• Interpreting and summarising data for documents.
• Managing stakeholder alignment and project timelines.

Skills

Medical writing

Stakeholder management

Project management

Leadership skills

Job description

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Medical Writer II - 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 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 will have the chance to take on project management responsibilities.

For this position, the client is seeking someone with experience as a medical writer and as a 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 on this position or similar opportunities, please contact Chanel Hicken at 0203 868 1011 or email your updated CV to [emailprotected]. We can arrange a confidential discussion on how you can get involved in this exciting opportunity.