🛠 Tech Stack

💼 About This Role

You'll support IRT management activities across clinical projects, ensuring alignment with sponsor requirements and regulatory standards. Your core impact includes maintaining system integrity, supporting study timelines, and contributing to successful project delivery. This role also drives operational excellence through process improvement.

🎯 What You'll Do

• Draft IRT-related documents using standard templates
• Assist in basic database testing to ensure system functionality
• Support User Acceptance Testing with cross-functional teams
• Provide user support and troubleshoot IRT system issues

📋 Requirements

• 1-3 years related experience in clinical trials
• Basic understanding of clinical trial processes and IRT systems
• Knowledge of GxP and ICH-GCP regulatory requirements
• Proficiency in IRT documentation like URS and UAT scripts

✨ Nice to Have

• Experience with eTMF systems
• Familiarity with drug supply logistics
• Cross-functional collaboration experience