Biostatistician II - Remote

Overview

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

In Short

• Generate randomization schedules.
• Assist with statistical methods review of clinical study protocols.
• Provide and/or 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 regulatory analyses.
• Review statistical sections of clinical study reports.
• Interact with sponsors and project managers.
• Train and mentor new biostatisticians.

Requirements

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

Benefits

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