Principal Statistician

Job Summary

Working remotely in a full-time capacity, the Principal Statistician will contribute to statistical activities for global clinical trials, acting as a project lead while collaborating with international teams of statisticians, programmers, and data managers.

Key responsibilities

• Conduct statistical analyses for clinical trials, including interim and final analyses, and develop study protocols and statistical analysis plans
• Review statistical deliverables and provide training for statisticians and SAS programmers
• Act as a communication line for project teams and participate in audits and bid defense meetings

Required qualifications

• MSc in Statistics or equivalent
• Expert knowledge of statistical principles and methods used in clinical research
• Proficient in SAS programming and CDISC ADaM standards
• Experience with adaptive designs and sample size calculations
• Familiarity with relevant regulations and guidelines (e.g., FDA, EMA, ICH)