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

JR United Kingdom; Worcester; Remote; GBP 50,000 - 70,000; Full time

Job summary

A renowned global clinical research organisation seeks an experienced Senior Medical Writer for a home-based role in Worcester. You will play a pivotal role in authoring crucial clinical documents and leading multiple projects, guiding junior writers while ensuring high-quality submissions.

Qualifications

• Experience in Phase I-III protocol and CSR medical writing.
• Skills in stakeholder management, both internal and external.
• Experience as a project manager or project lead.

Responsibilities

• Authoring high-complexity study-level documents including protocols and meeting packages.
• Independently author clinical evaluation plans, reports, and other documents for regulatory submissions.
• Supervising or guiding junior medical writers.

Skills

Medical Writing

Stakeholder Management

Project Management

Job description

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

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 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 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 or guiding junior medical writers.

For this position, the client is seeking someone with:

• Experience in Phase I-III protocol and CSR medical writing
• Stakeholder management skills, both internal and external
• Project management and project lead experience

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