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

JR United Kingdom; Leicester; Remote; GBP 40,000 - 70,000; Full time

Job summary

A leading global clinical research organisation in Leicester seeks a Senior Medical Writer to prepare complex clinical documents and lead writing projects. You will author study protocols, evaluations, and regulatory submissions while guiding junior writers. This role is pivotal in delivering key therapies to market, requiring robust medical writing experience and leadership skills.

Qualifications

• Experience as a medical writer and project lead on medical writing projects.
• Experience in writing Phase I - III protocols and CSRs.
• Ability to manage stakeholders effectively.

Responsibilities

• Author high-complexity study-level documents including protocols and investigator brochures.
• Lead multiple projects and supervise junior medical writers.
• Develop clinical evaluation plans and reports for regulatory submissions.

Skills

Medical Writing

Project Management

Stakeholder Management

Leadership

Education

Bachelor’s or Master’s degree in a relevant field

Job description

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

Client: Planet Pharma

Location: Leicester, UK

Job Category: Other

EU work permit required: Yes

Job Views:

1

Posted:

06.06.2025

Expiry Date:

21.07.2025

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) that is looking for an experienced Medical Writer to join the team and support the preparation of submission and other complex clinical documents.

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

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

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

Candidates should have experience as a medical writer and project lead on medical writing projects.

Additional desired experience includes:

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

For more information or to discuss this opportunity, please contact Chanel Hicken at 0203 868 1011 or email your updated CV to [emailprotected]. We look forward to arranging a confidential discussion about how you can join this exciting role.