Statistical Programming Associate Director

Job Summary

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

Key Responsibilities

• Support project leads on outsourced programming activities and ensure effective vendor programming implementation
• Provide hands-on statistical programming support for regulatory submissions and develop submission data packages
• Develop and maintain programming standards and tools to enhance programming efficiency and quality

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 with SAS macro and/or system utility development preferred
• Advanced knowledge of CDISC SDTM and ADaM, and their implementation in clinical trials analysis preferred
• Understanding of statistical concepts and advanced statistical methods using SAS and R preferred