IRT Coordinator

Job Summary

A company is looking for an IRT Coordinator to support core IRT management activities across clinical projects.

Key Responsibilities

• Assist in IRT documentation preparation and database testing for clinical trials
• Support User Acceptance Testing (UAT) and trial drug inventory management
• Contribute to continuous improvement initiatives and maintain study documentation in the eTMF

Required Qualifications

• Post-secondary diploma/certificate with 1-3 years of related experience
• Basic understanding of clinical trial processes and IRT systems
• Knowledge of GxP, ICH-GCP, and regulatory compliance requirements
• Experience in cross-functional collaboration with clinical operations and data management
• Proficiency in managing IRT system documentation and project coordination skills