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

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

Job summary

A global clinical research organization is seeking a Medical Writer II for a home-based position in the UK. The role involves authoring clinical documents, managing tasks, and stakeholder coordination while contributing to crucial therapy submissions. Ideal candidates will possess medical writing experience across phases I to III and have strong project management skills.

Qualifications

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

Responsibilities

• Authoring study-level documents such as protocols and investigator brochures.
• Interpreting and summarising data.
• Managing medical writing tasks and stakeholder alignment.

Skills

Stakeholder management

Project management

Leadership

Job description

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

Client: Planet Pharma

Location: Portsmouth, Hampshire, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views: 2

Posted: 04.06.2025

Expiry Date: 19.07.2025

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) seeking an experienced Medical Writer to support the preparation of submission and other complex clinical documents.

Responsibilities include:

• Authoring study-level documents such as protocols, ICFs, lay summaries, briefing packages, and investigator brochures
• Interpreting and summarising data
• Managing medical writing tasks, stakeholder alignment, coordination, and adherence to timelines
• Representing medical writing in relevant project groups

This role offers the opportunity to join a renowned CRO and contribute to bringing therapies to market across various therapeutic areas. You will be assigned to one sponsor and may take on project management responsibilities.

Requirements include:

• Experience as a medical writer with Phase I - III protocol and CSR medical writing
• Stakeholder management skills (internal and external)
• Project management and leadership skills

For more information, contact Chanel Hicken at 0203 868 1011 or email your updated CV to [emailprotected] for a confidential discussion about this opportunity.