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

JR United Kingdom; Northampton; Remote; GBP 35,000 - 55,000; Full time

Job summary

A leading global clinical research organisation is seeking an experienced Medical Writer II to support the preparation of complex clinical documents. The role includes authoring study-level documents, managing tasks, and potentially overseeing project management responsibilities within a collaborative environment.

Qualifications

• Experience as a medical writer, specifically in Phase I - III protocols and CSRs.
• Background in managing medical writing projects as a project lead.

Responsibilities

• Authoring clinical documents such as protocols, ICFs, and investigator brochures.
• Summarising data and managing writing tasks with coordination.
• Representing medical writing in project groups.

Skills

Stakeholder Management

Project Management

Data Interpretation

Job description

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

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.

In this role, you will be responsible for authoring study-level documents including protocols, ICFs, lay summaries of clinical trial results, briefing packages, and investigator brochures. Your responsibilities will also include:

1. Interpreting and summarising data
2. Managing medical writing tasks with stakeholder alignment, coordination, and adherence to timelines
3. Representing medical writing in relevant project groups

This is an exciting opportunity to join a renowned CRO and contribute to bringing key therapies to market across various therapeutic areas. You will be assigned to a single sponsor and may take on project management responsibilities.

The ideal candidate will have experience as a medical writer, including working as a project lead on medical writing projects, with specific experience in Phase I - III protocol and CSR medical writing, stakeholder management, and project management skills.

For more information or to apply, please contact Chanel Hicken at 0203 868 1011 or email your updated CV to [emailprotected]. We look forward to discussing how you can be part of this exciting opportunity.