Trial Master File Representative (Remote - UK)

11 hours, 33 minutes ago
Full-time
Junior
Technical Writing and Documentation
Celerion

Celerion

Celerion is a pioneer in early clinical research, offering Applied Translational Medicine services worldwide to expedite drug development processes.

Pharmaceuticals
251-1K
Founded 2010

Description

  • Prepare Trial Master Files for internal and external studies to sponsor-negotiated specifications.
  • Maintain Trial Master Files throughout the study lifecycle.
  • Create and maintain file structures and index TMF contents.
  • Ensure TMF completeness and document control for contracted TMF services.
  • Communicate with client sponsors, project managers, monitors, sites, and other study contacts.
  • Support compliance with protocol, regulatory, and local requirements.
  • Coordinate TMF-related activities across multiple studies and priorities.

Requirements

  • Bachelor's degree in a related field such as science or another biomedical discipline.
  • Experience in clinical research and/or Trial Master Files is preferred.
  • Minimum 1 year of document management experience.
  • Excellent interpersonal and oral and written communication skills.
  • Highly organized and collaborative.
  • Proficient with MS Word, Excel, and PowerPoint.
  • Ability to manage multiple priorities.
  • Must have full and permanent right to work in the UK.
  • Remote/home-based position within the UK.

Benefits

  • Competitive salary.
  • Strong developmental environment.
  • Remote, home-based role within the UK.

Interested in this position?

Apply directly on the company website

Apply Now

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