🛠 Tech Stack

💼 About This Role

You'll lead statistical strategy for clinical trials across therapeutic areas at a global CRO. You'll provide statistical support for Phase I–IV trials, regulatory submissions, and cross-functional collaboration. This permanent role offers the stability of a large organization with diverse sponsor exposure.

🎯 What You'll Do

• Provide statistical support for Phase I–IV clinical trials
• Develop Statistical Analysis Plans and TLF shells
• Perform statistical analyses and interpret results
• Support regulatory submissions and health authority queries

📋 Requirements

• Master’s or PhD in Statistics or related field
• 5–8 years biostatistics experience in CRO or pharma
• Proficiency in SAS and/or R programming
• Knowledge of CDISC standards (SDTM/ADaM)

✨ Nice to Have

• Experience supporting regulatory submissions
• Experience mentoring junior statisticians
• Familiarity with multiple therapeutic areas

🎁 Benefits & Perks

• 🏥 Health insurance
• 🏖️ Unlimited PTO
• 📈 Career growth opportunities
• 🌍 Remote flexibility
• 💰 Competitive compensation

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Phone Screen· 30 min
2. 2Technical Interview· 60 min
3. 3Hiring Manager Interview· 45 min