🛠 Tech Stack

💼 About This Role

You'll coordinate site activation activities for global clinical trials, ensuring regulatory compliance and timely delivery. You'll support study documentation management within eTMF systems and mentor junior team members. This fully remote role offers strong career growth in an international clinical research environment.

🎯 What You'll Do

• Coordinate site activation activities and ensure timeline adherence
• Prepare and maintain essential regulatory and clinical documentation
• Serve as communication point between sites, project teams, and CRAs
• Monitor project timelines, site progress, and payment reconciliation

📋 Requirements

• Bachelor's degree in life sciences or related field
• 2+ years of clinical research project coordination experience
• Experience supporting site start-up in global/multi-regional studies
• Strong understanding of GCP and regulatory requirements

✨ Nice to Have

• Experience with regulatory submissions and audit preparation
• Additional European or Asian language skills
• Vendor coordination experience

🎁 Benefits & Perks

• 🏠 Fully remote work within European locations
• ⏰ Flexible schedule for work-life balance
• 📈 Career advancement opportunities
• 📚 Ongoing training and professional development
• 🌍 International clinical research exposure

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter phone screen· 30 min
2. 2Hiring manager interview· 45 min
3. 3Technical interview or case study· 60 min