💼 About This Role

You'll manage clinical trial sites to ensure compliance with ICH-GCP and regulatory requirements. Your work ensures data integrity, patient safety, and smooth study execution. This role offers the chance to contribute to global drug development.

🎯 What You'll Do

• Conduct site qualification, initiation, monitoring, and close-out visits
• Ensure compliance with ICH-GCP, study protocols, and regulations
• Verify informed consent and protect subject confidentiality
• Review source documents, case report forms, and resolve data queries

📋 Requirements

• Bachelor's degree in health or science field
• Understanding of ICH-GCP guidelines and regulations
• Experience in clinical monitoring or research roles
• Willingness to travel up to 75%

✨ Nice to Have

• CRA experience preferred
• Strong knowledge of source data verification
• Proficiency with clinical systems

🎁 Benefits & Perks

• 💰 Competitive compensation
• 🌍 Global clinical trials impact
• 📈 Career development and training
• 🏖️ Flexible work arrangements
• ❤️ Comprehensive benefits package

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter screen· 30 min
2. 2Hiring manager interview· 45 min
3. 3Technical assessment· 60 min
4. 4Offer· 15 min