🛠 Tech Stack

💼 About This Role

You'll lead statistical activities for clinical trials across multiple therapeutic areas at a global CRO. Your work directly supports regulatory submissions for early- and late-stage studies. This role offers the stability of a single sponsor with the career growth of a large CRO.

🎯 What You'll Do

• Contribute to design of early/late-stage protocols
• Develop and write statistical analysis plans
• Perform statistical analyses for interim and final reports
• Support submission activities including integrated summaries

📋 Requirements

• MS or PhD in Statistics or Biostatistics
• PhD +4 years or MS +9 years clinical trial experience
• Hands-on Phase I/II/III clinical trial experience
• Proficient in SAS programming

✨ Nice to Have

• Excellence in R programming
• Experience with regulatory submissions in US, Europe, Japan, ROW

🎁 Benefits & Perks

• 🌍 Remote work across WEU
• 🏢 Global CRO with strong quality focus
• 📈 Career development opportunities
• 🤝 Supportive culture and low turnover

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Phone Screen· 30 min
2. 2Technical Interview· 60 min
3. 3Offer· 1 week