Senior Biostatistician

Job Summary

Senior Biostatistician, responsible for leading the statistical aspects of clinical studies and regulatory filings in a full-time, salaried position.

Key Responsibilities

• Lead and optimize clinical study designs, endpoints, and analysis strategies
• Develop statistical programs and write statistical analysis plans for clinical trials
• Collaborate with cross-functional teams and oversee external vendor deliverables

Required Qualifications

• 4 years of experience, or PhD in a relevant field
• Proficient in SAS and R programming, with knowledge of CDISC standards
• Experience with clinical trial design and analysis, including complex statistical methods
• Knowledge of regulatory requirements and guidelines, such as ICH Guidelines
• Familiarity with Bayesian and adaptive design preferred