🛠 Tech Stack

💼 About This Role

You'll coordinate site activation and study operations for global clinical trials across multiple therapeutic areas, ensuring regulatory compliance and timely delivery. This fully remote role offers strong career growth within a globally connected clinical research environment.

🎯 What You'll Do

• Coordinate site activation and regulatory documentation for clinical trials
• Serve as communication point between clinical sites, project teams, and CRAs
• Maintain eTMF and track study timelines, enrollment, and payments
• Support audits, inspections, and process improvement initiatives

📋 Requirements

• Bachelor's degree in clinical research, life sciences, or healthcare
• 2+ years of Project Coordinator experience in clinical research
• Experience supporting site start-up and global clinical trials
• Knowledge of GCP and regulatory requirements

✨ Nice to Have

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

🎁 Benefits & Perks

• 🏠 Fully remote work within Europe
• ⏰ Flexible schedule supporting work-life balance
• 📈 Ongoing training and professional development
• 🌍 Exposure to international clinical research projects

📨 Hiring Process

Estimated timeline: 1-2 weeks · AI estimate

1. 1Recruiter phone screen· 30 min
2. 2Hiring manager interview· 45 min
3. 3Offer· 1 day