🛠 Tech Stack

💼 About This Role

You'll coordinate site activation activities for global clinical trials, ensuring timelines and regulatory compliance. You'll serve as a key communication link between sites, project teams, and CRAs. This fully remote role offers strong career growth in a globally connected environment.

🎯 What You'll Do

• Coordinate site activation and regulatory documentation.
• Prepare investigator sites for study initiation.
• Serve as key communication point between sites and teams.
• Maintain eTMF and project tracking systems.

📋 Requirements

• Bachelor's degree in life sciences or related field.
• 2+ years as Project Coordinator in clinical research.
• Experience with site start-up and global studies.
• Knowledge 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 European locations.
• ⏰ Flexible work schedule.
• 📚 Ongoing learning and development.
• 🌍 Exposure to international clinical research.
• 📈 Career advancement opportunities.

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter Screen· 30 min
2. 2Hiring Manager Interview· 45 min
3. 3Technical/Skills Assessment· 60 min