Senior statistical programmer / principal statistical programmer

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, ADa M, 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, ADa M, TLFs, and regulatory submissions.
- Good understanding of CDISC standards and clinical trial processes.
Leadership Requireme...