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

JR United Kingdom

Liverpool

Remote

GBP 55,000 - 80,000

Full time

Yesterday
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Job summary

A leading global clinical research organisation seeks a Senior Medical Writer to join their Liverpool team on a home-based role. The ideal candidate will be responsible for authoring complex clinical documents and leading projects, contributing significantly to bringing critical therapies to market.

Qualifications

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

Responsibilities

  • Author high-complexity study-level documents including protocols and meeting packages.
  • Lead multiple projects and supervise junior medical writers.
  • Independently author clinical evaluation plans and regulatory submissions.

Skills

Project management
Stakeholder management
Leadership skills

Job description

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

Planet Pharma is currently working with a global clinical research organisation (CRO) 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 summaries and overview documents in CTD/eCTD formats for global regulatory submissions

This role offers the 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, leading multiple projects, and supervising junior medical writers.

Requirements include experience as a medical writer, project lead experience 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, contact Chanel Hicken at 0203 868 1011 or email your updated CV to [emailprotected]. We can arrange a confidential discussion about this exciting opportunity.

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