Associate Director, Statistical Programming

Job Summary

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

Key Responsibilities

• Provide statistical programming support for regulatory submissions and oversee programming technical decisions
• Develop programming standards and templates to enhance efficiency and quality in clinical trial data analysis
• Evaluate and improve the computing environment system for programming and analysis efficiency

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 analysis of clinical trials with a Bachelor's degree; 7+ years with a Master's degree
• Experience in SAS macro and/or 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 related to clinical trials preferred