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

JR United Kingdom; Lincoln; On-site; GBP 50,000 - 75,000; Full time

Job summary

Join a leading global clinical research organisation as a Senior Medical Writer in Lincoln. This role involves authoring critical clinical documents and leading projects, contributing to the development of key therapies across various therapeutic areas. Ideal candidates should have significant medical writing experience and project leadership skills.

Qualifications

• Experience as a medical writer and project lead.
• Phase I - III protocol and CSR medical writing experience required.
• Strong interpersonal skills for working with stakeholders.

Responsibilities

• Author high-complexity study-level documents including protocols and investigator brochures.
• Lead multiple projects and supervise junior writers.
• Manage internal and external stakeholder relationships.

Skills

Stakeholder management

Project management

Leadership

Job description

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

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 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.

Ideal candidates will have experience as a medical writer and project lead on medical writing projects, with:

• Phase I - III protocol and CSR medical writing experience
• Stakeholder management skills, both 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 contribute to this exciting role.