🛠 Tech Stack

💼 About This Role

You'll coordinate site activation and study operations for global clinical trials in a remote European team. You'll ensure regulatory compliance and timely project delivery while mentoring junior team members.

🎯 What You'll Do

• Coordinate site activation activities for clinical trials
• Prepare investigator sites by reviewing essential documentation
• Maintain study documentation in eTMF and tracking systems
• Monitor project timelines and site activation progress

📋 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
• Strong understanding of GCP and regulatory requirements

✨ Nice to Have

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

🎁 Benefits & Perks

• 🏠 Fully remote work opportunity
• 🕒 Flexible schedule supporting work-life balance
• 📚 Training and development opportunities
• 🌍 International projects and collaboration
• 📈 Career advancement in a growing organization

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter call· 30 min
2. 2Hiring manager interview· 45 min
3. 3Technical interview· 60 min