Associate Director Statistical Programming - job 1 of 2

Job Summary

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

Key Responsibilities

• Provide statistical programming support for regulatory submissions and ensure compliance with CDISC standards
• Develop and maintain programming standards, templates, and tools to enhance efficiency and quality
• Evaluate and improve the computing environment for statistical programming and 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 in statistical analysis of clinical trials with a Bachelor's degree; 7+ years with a Master's degree
• Experience with SAS macro and system utility development preferred
• Advanced knowledge of CDISC SDTM and ADaM standards and their implementation in clinical trials
• Strong understanding of statistical concepts and methods relevant to clinical trial analysis