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

JR United Kingdom; Basingstoke; Remote; GBP 45,000 - 70,000; Full time

Job summary

A global clinical research organization is seeking a Senior Medical Writer to prepare complex clinical documents, contribute to regulatory submissions, and manage multiple projects. This role involves collaborating with various stakeholders and mentoring junior writers, offering an exciting opportunity to advance in a dynamic environment.

Qualifications

• Experience as a medical writer with Phase I - III protocol and CSR medical writing.
• Experience in managing projects and stakeholders.

Responsibilities

• Author high-complexity study documents including protocols and clinical evaluation plans.
• Lead multiple projects and supervise junior medical writers.

Skills

Stakeholder management

Project management

Job description

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Senior Medical Writer - Global Clinical Research Organisation - Home based in UK, Basingstoke

Client:

Planet Pharma

Location:

UK, Basingstoke

Job Category:

Other

EU work permit required:

Yes

Job Views:

1

Posted:

04.06.2025

Expiry Date:

19.07.2025

Job Description:

Senior Medical Writer - 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.

As Senior Medical Writer, you will author high-complexity study documents, including protocols, ICFs, investigator brochures, and meeting packages. You will also independently author:

• Clinical evaluation plans and reports
• Paediatric Investigational Plans (PIPs)
• Clinical summaries and overview documents in CTD/eCTD formats for global regulatory submissions

This is an exciting opportunity to join a renowned CRO and contribute to bringing therapies to market across various therapeutic areas. You will be assigned to one sponsor, leading multiple projects, and supervising junior medical writers.

Requirements include:

• Experience as a medical writer with Phase I - III protocol and CSR medical writing
• Stakeholder management skills, both internal and external
• Project management/project lead experience

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