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

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

Job summary

Join a leading global clinical research organisation as a Senior Medical Writer based in Shrewsbury. In this role, you'll lead multiple projects and contribute to bringing essential therapies to market. As part of a collaborative team, you'll author critical clinical documents required for regulatory submissions. Ideal candidates will possess extensive medical writing experience in diverse phases, including stakeholder management and project leadership.

Qualifications

• Experience as a medical writer, particularly in Phase I-III protocols and CSR.
• Strong stakeholder management skills, both internal and external.
• Project management and leadership skills.

Responsibilities

• Author high-complexity study-level documents including protocols and ICFs.
• Independently create clinical evaluation plans and reports.
• Supervise and guide junior medical writers.

Skills

Stakeholder management

Project management

Leadership

Job description

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

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.

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 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 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.

Requirements include:

• Experience as a medical writer, particularly in Phase I-III protocols and CSR medical writing
• Stakeholder management skills, both internal and external
• Project management and leadership skills

For more information, please contact Chanel Hicken at 0203 868 1011 or email your updated CV to [emailprotected]. We can arrange a confidential discussion on how you can get involved in this exciting opportunity.