🛠 Tech Stack

💼 About This Role

You'll join a global CRO to support a single sponsor, contributing to early/late-stage clinical trial design and statistical analysis across multiple therapeutic areas. Your work will directly impact regulatory submissions and integrated safety/efficacy summaries. This role offers a consultative, independent work environment with exposure to diverse therapeutic areas and global submissions.

🎯 What You'll Do

• Contribute to protocol design for early/late-stage trials across therapies
• Develop and write statistical analysis plans (SAPs)
• Perform statistical analyses for interim and final regulatory 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, and Rest of World

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

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