Job Summary

• Perform daily administrative activities to ensure a complete and accurate Trial Master File delivery.
• Assist Clinical Research Associates and Regulatory and Start-Up teams with document and system updates, tracking site compliance and performance.
• IQVIA is committed to integrity in its hiring process and maintains a zero tolerance policy for candidate fraud.

Matching Summary

Skills & Requirements

Key Requirements

• High School Diploma or equivalent
• 3 years administrative support experience
• Proficient in Microsoft Word, Excel, PowerPoint
• Awareness of GCP and ICH guidelines
• Knowledge of applicable protocol requirements

Work Rights