🛠 Tech Stack

💼 About This Role

You'll work on early/late-stage clinical trial designs across multiple therapeutic areas as a consultant for a global CRO's client. You'll draft protocols and statistical analysis plans, and perform analyses for regulatory submissions. This role offers the stability of a large CRO with the focus of a single sponsor.

🎯 What You'll Do

• Contribute to design of early/late-stage clinical trial protocols
• Develop and write statistical analysis plans (SAPs)
• Perform statistical analyses for interim/final reports
• Support submission activities including integrated safety/efficacy 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

🎁 Benefits & Perks

• 🏖️ Remote work flexibility
• 📈 Career development opportunities within a global CRO
• 🏥 Health insurance (typical for contractors)
• 💰 Competitive contract rate

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Submit CV / Application· N/A
2. 2Phone screen with recruiter· 30 min
3. 3Client interview· 60 min