Clinical Trial Documentation Associate

Job Summary

A company is looking for a Trial Documentation Associate I to support clinical trial activities.

Key Responsibilities

• Assist in maintaining clinical research operations and study documentation
• Collect, review, and maintain essential regulatory documents
• Track documentation and study status within CTMS and eTMF systems

Required Qualifications, Training, and Education

• Bachelor's degree in a relevant area required
• Prior experience with clinical research operations preferred
• Experience managing clinical trial regulatory documents preferred
• Experience in study start-up and site management preferred
• Trial Master File (TMF) set-up and maintenance experience preferred