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

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

Job summary

Une organisation de recherche clinique de renommée mondiale recherche un rédacteur médical senior basé à Glasgow pour contribuer à des projets cliniques majeurs. Le candidat idéal sera responsable de l'élaboration de documents cliniques complexes, dirigera des initiatives et supervisera d'autres rédacteurs. Ce poste offre l'opportunité de jouer un rôle essentiel dans le développement de thérapies critiques à travers divers domaines thérapeutiques.

Qualifications

• Expérience en rédaction médicale et en gestion de projets.
• Connaissances spécifiques en rédaction de protocoles et rapports cliniques.
• Aptitudes avérées en gestion des parties prenantes internes et externes.

Responsibilities

• Rédaction de documents cliniques complexes pour soumissions réglementaires.
• Direction de projets en supervisant et guidant des rédacteurs juniors.
• Rédaction des plans d'évaluation clinique et des résumés cliniques.

Skills

Rédaction médicale

Gestion de projet

Leadership

Gestion des parties prenantes

Job description

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

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 summaries and overview documents in CTD/eCTD formats for global regulatory submissions

This is an exciting opportunity to join a globally renowned CRO and contribute significantly to 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.

The ideal candidate will have experience as a medical writer and project lead on medical writing projects, with specific experience in:

• Phase I - III protocol and CSR medical writing
• Stakeholder management, 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 get involved in this exciting role.