Documentation Specialist

Job Summary

A company is looking for a Documentation Specialist who will support the management of program documentation in clinical research.

Key Responsibilities

• Support electronic Trial Master File (eTMF) setup, maintenance, and closeout
• Collaborate with internal project teams for timely document retrieval and filing
• Conduct quality checks and maintain systems for TMF document tracking

Required Qualifications

• Bachelor's degree preferred
• 1 - 2 years of experience in documentation management systems preferred
• Familiarity with clinical study documentation and GCP guidelines
• Experience with clinical trial electronic databases preferred
• Strong computer skills, including proficiency in Microsoft Office