💼 About This Role

You'll coordinate and support site activation activities across assigned clinical trials, ensuring timely study initiation. You'll manage essential documentation and collaborate with cross-functional teams to ensure compliance with global regulatory standards. This role contributes directly to delivering high-quality clinical research that supports new therapies.

🎯 What You'll Do

• Lead site activation from start-up through initiation and close-out
• Prepare Investigator Initiation Packages for site activation approval
• Manage essential documents for regulatory and ethics submissions
• Track site activation progress and update clinical trial systems

📋 Requirements

• 2+ years experience in clinical trials, ideally in site activation
• Bachelor's degree in life sciences or equivalent
• Strong knowledge of ICH-GCP guidelines and regulatory requirements
• Ability to manage multiple site activation workflows simultaneously

✨ Nice to Have

• Experience within a pharmaceutical company or CRO
• Multilingual ability is a plus

🎁 Benefits & Perks

• 🌍 Global clinical trials exposure
• 📈 Career development opportunities within clinical operations
• 🎓 Structured training in global clinical trial processes
• 🤝 Collaborative and mission-driven work environment
• 💰 Competitive compensation aligned with experience

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter Call· 30 min
2. 2Hiring Manager Interview· 45 min
3. 3Offer· 1 week