Senior / Principal Statistical Programmer

Experience

• Senior Statistical Programmer: 7+ years
• Principal Statistical Programmer: 9+ years

Role Summary

Responsible for end-to-end statistical programming activities for clinical studies, from specification creation through regulatory submissions, ensuring high-quality and compliant deliverables.

Key Responsibilities

• Develop and validate SDTM, ADaM, and TLFs.
• Create and review programming specifications.
• Support regulatory submissions and ensure CDISC compliance.
• Perform QC and maintain programming standards.
• Collaborate with cross-functional teams and support study deliverables.
• Contribute to process improvements and mentoring activities.

Required Skills

• Strong SAS programming expertise; R knowledge is a plus.