🛠 Tech Stack

💼 About This Role

You'll serve as a biostatistics lead for a global pharmaceutical client, managing complex clinical trials. You'll independently contribute to study design, protocol development, and regulatory submissions. This role offers long-term contract stability with the backing of a full-service CRO.

🎯 What You'll Do

• Design early/late-stage protocols across multiple therapeutic areas
• Develop and write statistical analysis plans
• Perform statistical analyses for interim and final reports
• Support regulatory submission activities including integrated summaries

📋 Requirements

• MS or PhD in Statistics or Biostatistics
• PhD + 6 years (or MS + 11 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

🎁 Benefits & Perks

• 🏖️ Remote work within Western EU
• 📅 24-month contract with potential extension
• 🏢 Global CRO with over 4,000 professionals

📨 Hiring Process

Estimated timeline: 2-3 weeks · AI estimate

1. 1CV submission· 1 day
2. 2Phone interview· 30 min
3. 3Client interview· 1 hour