Client-facing Principal Biostatistician Consultant on Oncology late-phase studies (remote).
Lead protocol development: study design, sample size, randomization, SAP.
Provide statistical oversight to studies and ensure data quality.
Mentor statisticians and coordinate project-wide statistics.

🎯 Requirements

MS or PhD in Statistics/Biostatistics or related field; PhD (2-4 yrs) or MS (5-7 yrs)
Strong SAS skills.
Oncology therapeutic area experience.
Pharma/CRO clinical trials with FDA interactions.
Strong oral and written communications skills.
Understanding of statistics, drug development, and FDA regulations.

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