🛠 Tech Stack

💼 About This Role

You'll lead biostatistics for complex clinical trials, mentoring junior staff and driving regulatory submissions. You'll collaborate on study designs from early to late-stage across therapeutic areas.

🎯 What You'll Do

• Contribute to protocol and statistical analysis plan development.
• Perform statistical analyses for interim and final reports.
• Support regulatory submissions with integrated safety/efficacy summaries.
• Lead study deliverables with statistical programmers and data managers.

📋 Requirements

• MS or PhD in Statistics or Biostatistics
• PhD + 6 years or MS + 11 years clinical trial experience
• Hands-on Phase I/II/III trial experience
• Proficient in SAS programming

✨ Nice to Have

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

🎁 Benefits & Perks

• 🌍 Global CRO with career opportunities
• 🤝 Supportive culture with focus on quality

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter screen· 30 min
2. 2Technical interview· 60 min
3. 3Client interview· 60 min

🚩 Heads Up

• 24-month contract with no permanent option mentioned