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

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

Job summary

A global clinical research organization offers an exciting opportunity for an experienced Medical Writer II based in High Wycombe. The role involves authoring crucial clinical documents and participating in project management, contributing to the development of key therapies globally.

Qualifications

• Experience as a medical writer and project lead.
• Familiarity with Phase I - III protocol and CSR medical writing.
• Strong project management and leadership skills.

Responsibilities

• Author study-level documents including protocols and investigator brochures.
• Interpret and summarize data for clinical documents.
• Coordinate medical writing tasks and manage stakeholder alignment.

Skills

Medical Writing

Stakeholder Management

Project Management

Job description

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

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.

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 have the chance to take on project management responsibilities.

For this position, the client is looking for 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, 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.