Senior Statistical Programmer Consultant

Job Summary

Serving as a senior technical expert, the remote Senior Statistical Programmer Consultant will lead programming activities for oncology clinical trials, manage timelines and deliverables, and ensure compliance with regulatory submissions while leveraging advanced expertise in SAS and CDISC standards.

Key Responsibilities

• Lead programming activities for oncology clinical trials and oversee production of Tables, Listings, and Figures (TLFs)
• Act as programming lead for assigned studies, coordinating with cross-functional teams and external vendors
• Prepare submission-ready programming outputs and documentation, ensuring compliance with regulatory requirements

Required Qualifications

• Bachelor's or Master's degree in Statistics, Computer Science, Mathematics, Life Sciences, or related field
• 8-12+ years of statistical programming experience in pharma/biotech or CRO
• Expert-level proficiency in SAS and strong understanding of CDISC SDTM and ADaM standards
• Significant experience supporting oncology clinical trials and regulatory submissions
• Ability to collaborate cross-functionally and manage complex programming deliverables