Trial Master File Representative

This is a fully remote position, open to applicants in United Kingdom.

📋 Description

• Prepare Trial Master Files (TMF) for both internal and external studies in accordance with Sponsor-negotiated specifications.

• Ensure the Trial Master Files are complete and accurate.

• Oversee the maintenance of the Trial Master File.

• Establish file structures and index contents effectively.

• Engage in communication with client Sponsors, Project Managers, monitors, sites, and other study contacts.

• Guarantee compliance with protocol and regulatory/local requirements.

⛳️ Requirements

• Bachelor's degree in a relevant field, such as science or another biomedical discipline.

• Preferred experience in clinical research and/or Trial Master Files.

• At least 1 year of experience in document management.

• Exceptional interpersonal and oral/written communication skills.

• Highly organized and able to work collaboratively.

• Proficient in computer applications, including MS Word, Excel, and PowerPoint.

• Capability to manage multiple priorities efficiently.

• Must possess full and permanent right to work in the UK.

• Celerion does not currently provide sponsorships.

🏝️ Benefits

• Competitive salary.

• Strong developmental environment.

• Equal Opportunity Employer.