Trial Master Files Specialist

A company is looking for a Trial Master Files Representative to manage and maintain Trial Master Files for clinical studies.

Key Responsibilities

Prepare and ensure the completeness of Trial Master Files (TMF) for internal and external studies

Maintain the TMF, including creating file structures and indexing contents

Communicate with client Sponsors and other study contacts to ensure compliance with protocols and regulatory requirements

Required Qualifications

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

Experience in clinical research and / or Trial Master Files preferred

Minimum 1 year of document management experience

Proficient computer skills, including MS Word, Excel, and PowerPoint