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.
- Hands-on experience with SDTM, ADaM, TLFs, and regulatory submissions.
- Good understanding of CDISC standards and cli...