Trial Master Files Representative

Summary

Join Celerion, a leader in clinical research, as a Full-Time Trial Master Files Representative! This remote position allows you to work from anywhere in the US. You will be responsible for preparing and ensuring the completeness of Trial Master Files (TMF) for internal and external studies, maintaining the TMF, creating file structures, and communicating with clients and study contacts to ensure compliance. The role requires a Bachelor's degree in a related field, experience in clinical research or TMF, and excellent communication and organizational skills. A competitive hourly rate is offered.

Requirements

• Bachelor's degree in related field such as science, nursing, or other biomedical discipline
• 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

Responsibilities

• Prepare and ensure the completeness of Trial Master Files (TMF) for internal and external studies
• Maintain the TMF
• Create file structures and index contents
• Communicate with client Sponsors, Project Managers, monitors, sites and other study contacts to ensure compliance to protocol, and regulatory/local requirements

Preferred Qualifications

Experience in clinical research and/or Trial Master Files