🛠 Tech Stack

💼 About This Role

You'll coordinate site activation activities for global clinical trials, ensuring regulatory compliance and timely delivery. Working with project managers and clinical teams, you'll maintain documentation and support study operations. This role offers remote work with exposure to international research projects.

🎯 What You'll Do

• Coordinate site activation and regulatory documentation
• Serve as communication point between sites and project teams
• Maintain eTMF and project tracking systems
• Monitor timelines, enrollment, and payment reconciliation

📋 Requirements

• Bachelor's degree in clinical research or life sciences
• Minimum 2 years as Project Coordinator in clinical research
• Experience with site start-up and global studies
• Understanding of GCP and regulatory requirements

✨ Nice to Have

• Experience with regulatory submissions
• Additional European or Asian language skills

🎁 Benefits & Perks

• 🏡 Remote work within European locations
• 🕒 Flexible schedule
• 📈 Career advancement opportunities
• 🎓 Ongoing training and development
• 💼 Permanent full-time employment

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter screen· 30 min
2. 2Hiring manager interview· 45 min
3. 3Technical/team interview· 60 min