Trial Master Files Representative

About the role

Celerion has an opportunity for a Full-Time Trial Master Files Representative to join our team. This is a remote, home-based position and may be filled from any US geography.

Responsibilities

• Involved in the preparation and completeness of the Trial Master Files (TMF) for internal and external studies where Celerion has been contracted for the TMF services to meet Sponsor negotiated specifications
• Responsible for maintenance of the TMF, creating a file structure and indexing contents
• Communicate with client Sponsors, Project Managers, monitors, sites and other study contacts to ensure compliance to protocol, and regulatory/local requirements

Requirements

• Bachelor's degree in related field such as science, nursing, or other biomedical discipline
• Experience in clinical research and/or Trial Master Files preferred
• Minimum 1 year document management experience
• Excellent interpersonal and oral/written communication skills
• Highly organized and collaborative
• Proficient computer skills, i.e., MS Word, Excel, PowerPoint
• Ability to manage multiple priorities

Celerion Values

• Integrity
• Trust
• Teamwork
• Respect