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

JR United Kingdom; Warrington; On-site; GBP 50,000 - 70,000; Full time

Job summary

A leading global clinical research organisation seeks a Senior Medical Writer to author complex clinical documents. This exciting opportunity involves leading multiple projects for one sponsor, managing stakeholders, and guiding junior writers, focusing on bringing key therapies to market.

Qualifications

• Experience as a medical writer and project lead on medical writing projects.
• Experience with Phase I - III protocol and CSR medical writing.

Responsibilities

• Authoring high-complexity study-level documents including protocols and investigator brochures.
• Leading multiple projects and supervising junior medical writers.

Skills

Project management

Stakeholder management

Leadership

Job description

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

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 be responsible for independently authoring:

• 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 play a significant role in bringing key therapies to market across various therapeutic areas. You will be assigned to one sponsor, leading multiple projects, and supervising and guiding junior medical writers.

For this position, the client is seeking someone with experience as a medical writer and project lead on medical writing projects.

Experience with:

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

For more information or similar opportunities, 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.