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

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

Job summary

A globally renowned CRO is seeking a Medical Writer II to join their team in London. This role involves authoring key clinical documents, managing projects, and working closely with stakeholders. Ideal candidates will have significant experience in medical writing and project leadership, providing an exciting opportunity to contribute to vital clinical research efforts.

Qualifications

• Experience as a medical writer with project lead skills.
• Phase I - III protocol and CSR writing experience.
• Ability to interpret and summarise data.

Responsibilities

• Authoring study-level documents including protocols and investigator brochures.
• Coordinating medical writing tasks and adhering to timelines.
• Representing medical writing in project groups.

Skills

Medical writing

Stakeholder management

Project management

Job description

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

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 opportunity to take on project management responsibilities.

For this position, the 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 experience
• Stakeholder management - both internal and external
• Project management/project lead 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.