Associate Director Statistical Programming

This job has been removed
Location: Remote
Compensation: To Be Discussed
Reviewed: Fri, May 16, 2025
This job expires in: 9 days
SAS SDTM ADaM TFLs

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
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