Protocol development for study design, sample size, randomization, and SAP.
Statistical oversight to ensure quality and alignment with project requirements.
Ensure data for analyses are complete, accurate, and consistent.
Statistical analysis plans and timely input into reports.
Mentor peers and coordinate statisticians across projects to deliver on time.
Ensure accuracy and consistency of statistical tables, figures, and listings.

🎯 Requirements

MS or PhD in Statistics/Biostatistics or related; PhD w/ 2-3 yrs or MS w/ 5-6 yrs.
Strong Hematology/Oncology TA experience.
Excellent oral and written communication with clients.
Knowledge of statistics, drug development, and FDA regulations.
Pharma/CRO clinical trials exp; FDA interactions.
Experience mentoring statisticians and leading project teams.

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