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

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

Job summary

Join a leading global clinical research organization as a Medical Writer II. You will be pivotal in authoring essential clinical documents, guiding projects from inception to completion. This home-based role offers the chance to work with stakeholders across various therapeutic areas, ensuring vital therapies reach the market. Ideal for experienced writers looking to leverage their skills in a dynamic setting.

Qualifications

• Experience as a medical writer required.
• Familiarity with Phase I - III protocol and CSR medical writing.
• Project lead experience on medical writing projects.

Responsibilities

• Author study-level documents including protocols and investigator brochures.
• Interpret and summarize data for clinical documents.
• Handle medical writing aspects of task finalization.

Skills

Data interpretation

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, Bradford

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 submissions 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. You will also:

• Interpret and summarize data
• Handle medical writing aspects of task finalization, including stakeholder alignment, coordination, and adherence to timelines
• Represent 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 one sponsor and have the chance to take on project management responsibilities.

Requirements include experience as a medical writer, project lead on medical writing projects, and familiarity with:

• Phase I - III protocol and CSR medical writing
• Stakeholder management (internal and external)
• Project management and leadership skills

For more information or to apply, please contact Chanel Hicken at 0203 868 1011 or email your updated CV to [emailprotected]. We can arrange a confidential discussion about this exciting opportunity.