🛠 Tech Stack

💼 About This Role

You'll lead biostatistics functions for complex clinical studies across multiple therapeutic areas. You'll independently design protocols, develop statistical analysis plans, and perform analyses for regulatory submissions. This role offers the stability of a global CRO with the focus of a single sponsor.

🎯 What You'll Do

• Design early/late-stage protocols and draft amendments
• Develop and write statistical analysis plans
• Perform statistical analyses for interim/final regulatory reports
• Support submission activities including integrated safety/efficacy 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, Rest of World

🎁 Benefits & Perks

• 🌍 Global CRO with career opportunities
• 👥 Supportive culture and below-average turnover
• 📈 Professional development and continuous training
• 🎯 High-trust environment with client counterparts

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Submit CV· 1 day
2. 2Phone Interview· 30 min
3. 3Client Interview· 1 hour