Remote, home-based TMF role within the UK.
Prepare and maintain Trial Master Files (TMF) for internal/external studies.
Create file structures and index contents; ensure regulatory and protocol compliance.
Communicate with Sponsors, Project Managers, monitors, sites, and study contacts.

🎯 Requirements

Bachelor's degree in related field such as science or biomedical discipline.
Experience in clinical research and/or TMF preferred.
Minimum 1 year document management experience.
Excellent interpersonal and verbal/written communication skills.
Highly organized and collaborative.
Proficient MS Word, Excel, PowerPoint.

🎁 Benefits

Join a performance-driven drug research company.
Remote, UK-based position with competitive salary.

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