🛠 Tech Stack

💼 About This Role

You'll support core IRT management activities across clinical projects, ensuring alignment with sponsor requirements and regulatory standards. You'll collaborate cross-functionally to maintain system integrity and support study timelines. This role offers the chance to contribute to continuous process improvement and operational excellence in a remote setting.

🎯 What You'll Do

• Draft IRT documentation using standard templates
• Support database testing and User Acceptance Testing
• Assist with trial drug inventory management and ordering
• Generate and review report outputs for accuracy

📋 Requirements

• 1-3 years related experience
• Knowledge of GxP and ICH-GCP
• Proficiency in IRT system documentation (URS, UAT scripts)
• Strong project coordination skills

✨ Nice to Have

• Experience with IRT systems like IVRS/IWRS
• Familiarity with eTMF systems
• Experience in clinical trial supply chain

🎁 Benefits & Perks

• 🏖️ Remote work flexibility
• 🏥 Health insurance
• 📚 Professional development opportunities