🛠 Tech Stack

💼 About This Role

You'll coordinate site activation activities and manage essential documentation for global clinical trials. Your core impact is ensuring operational excellence and regulatory compliance across study phases. This role offers strong career growth within a fully remote, globally connected team.

🎯 What You'll Do

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

📋 Requirements

• Bachelor's degree in life sciences or related field
• 2+ years of project coordination in clinical research
• Experience with site start-up and global studies
• Understanding of GCP and regulatory requirements

✨ Nice to Have

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

🎁 Benefits & Perks

• 🏖️ Fully remote work within Europe
• ⏰ Flexible work schedule
• 📈 Career advancement opportunities
• 🎓 Ongoing training and professional development
• 🌍 International clinical research exposure

📨 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