Biostatistician - Remote

Overview

Provide statistical support for all phases of clinical development, including reviewing statistical sections of protocols, writing statistical analysis plans, and developing SAS programs for clinical trial data analysis.

In Short

• Generate randomization schedules.
• Assist with statistical methods review of clinical study protocols.
• Provide and verify sample size calculations.
• Author statistical analysis plans.
• Generate analysis datasets, tables, figures, and listings using SAS.
• Assist with quality control for statistical SAS programs.
• Provide programming support for exploratory analyses.
• Review output across programs for consistency.
• Train and mentor new biostatisticians.
• Work directly with sponsors and project managers.

Requirements

• Master's degree in Statistics, Biostatistics, or related field with 2+ years experience; PhD preferred.
• Experience with SAS.
• Knowledge of ICH guidelines and FDA regulations.
• Understanding of statistical concepts and techniques.
• Excellent organizational and communication skills.

Benefits

• Discretionary annual bonus.
• Health insurance.
• Retirement savings benefits.
• Life insurance and disability benefits.
• Paid time off for sick leave and vacation.