Principal Biostatistician

Job Summary

Working remotely on a full-time basis, the Principal Biostatistician will implement diverse statistical tasks throughout the clinical trial process, from study design to final analysis, while collaborating closely with clients in the pharmaceutical industry.

Key responsibilities

• Conduct statistical analyses and develop statistical analysis plans for clinical trials
• Collaborate with clinical leadership to design studies and write protocols
• Manage multiple clinical trials, ensuring compliance with regulatory standards and quality assurance

Required qualifications

• PhD or MS in Biostatistics, Statistics, or Mathematics; PhD is highly preferred
• Minimum of 10 years of experience as a study lead in clinical trials
• Experience with study design, protocol writing, and statistical analysis plan development
• Strong statistical modeling experience and expert-level proficiency in SAS programming
• Experience working with regulatory authorities (FDA, NIH, EMA, etc.) is preferred