Senior Manager Statistical Programming

Job Summary

Senior Manager Statistical Programming will work full-time in a remote/hybrid setting, leading statistical programming activities for clinical studies, ensuring high-quality deliverables, and providing programming expertise in compliance with project strategies and CDISC standards.

Key Responsibilities

• Lead statistical programming activities for multiple studies/projects, ensuring timely and high-quality deliverables
• Develop and maintain programming documentation and oversee the creation of SDTM and ADaM datasets
• Support global regulatory submissions and mentor junior programmers

Required Qualifications

• Minimum Bachelor's degree in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline
• 10+ years of programming experience in clinical trial data processing within the biotechnology, pharmaceutical, CRO, or healthcare industry
• Proficiency in SAS programming; knowledge of R or Python is a plus
• Strong understanding of pharmaceutical clinical development and regulatory submissions
• Experience with CDISC standards and regulatory guidance