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

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

Job summary

A leading global clinical research organization is seeking an experienced Medical Writer II to join their home-based team in Bath. You will be responsible for authoring critical clinical documents and managing projects. This role involves collaboration with various stakeholders and offers an exciting opportunity to impact the therapeutic market significantly.

Qualifications

• Experience in writing Phase I - III protocols and CSRs.
• Proven project lead experience.
• Ability to manage stakeholders effectively.

Responsibilities

• Author study-level documents including protocols, ICFs, and investigator brochures.
• Interpret and summarize clinical data.
• Lead and manage project timelines and stakeholder coordination.

Skills

Medical writing

Stakeholder management

Project management

Education

Experience as a Medical Writer

Job description

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

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 will have the chance to take on project management responsibilities.

The ideal candidate will have experience as a medical writer and have worked as a project lead on medical writing projects.

Required experience includes:

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