Associate Director, Statistical Programming - job 1 of 3

Job Summary

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

Key Responsibilities

• Support project leads and provide statistical programming expertise for outsourced projects, ensuring quality and compliance of datasets and TLFs
• Deliver hands-on statistical programming support for regulatory submissions, including the development of submission data packages and 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; Master's degree preferred
• 10+ years of experience in the pharmaceutical industry or CROs with a Bachelor's degree; 7+ years with a Master's degree
• Experience in SAS macro and system utility development preferred
• Advanced knowledge of CDISC SDTM and ADaM implementation in clinical trials
• Understanding of statistical concepts and drug development phases preferred