onsite
Principal Statistical Programmer
Software Engineer
Lead advanced statistical programming for clinical trials, driving ADaM dataset creation and CDISC compliance using SAS and cutting‑edge data analysis techniques.
About the role
Key Responsibilities
- Design, develop, and maintain ADaM datasets and SAS programs for clinical trial data analysis.
- Ensure CDISC standards compliance across all deliverables, including CRF and statistical analysis plans.
- Collaborate with biostatisticians, data managers, and clinical teams to translate study protocols into robust statistical outputs.
- Mentor junior programmers, providing technical guidance and code reviews.
- Lead troubleshooting and optimization of complex SAS code for performance and accuracy.
Requirements
- Extensive experience (10+ years) in statistical programming within a clinical research environment.
- Deep expertise in SAS, ADaM, and CDISC standards.
- Strong analytical skills with a proven track record of delivering high‑quality statistical reports.
- Excellent communication and teamwork abilities.
Skills
software developmentsystem designproblem solving