Associate Director Statistical Programming

Job Summary

A company is looking for an Associate Director, Evidence Generation Statistical Programming.

Key Responsibilities

• Provide statistical programming technical support for project teams and oversee programming deliverables
• Support regulatory submission processes by developing programming strategies and conducting analyses
• Develop and maintain programming standards and tools to enhance efficiency and quality in clinical trial data analysis

Required Qualifications

• Bachelor's degree in a science or technical field preferred; Master's degree preferred
• 10+ years of experience in the pharmaceutical industry or CROs supporting statistical programming, or 7+ years with a Master's degree
• Experience with SAS macro and system utility development preferred
• Advanced knowledge of CDISC SDTM and ADaM, with extensive implementation experience in clinical trials analysis preferred
• Strong understanding of statistical concepts and methodologies used in clinical trials