Principal Statistical Programmer
Core
Develop and validate complex analysis datasets, tables, listings, and figures for clinical study reports and regulatory submissions using SAS.
Role type
Principal Statistical Programmer (Clinical Trials)
Builds
Analysis datasets, tables, listings, figures, and graphs for regulatory submissions
Domain
Medical Technology / Clinical Research / Biostatistics
Deliverable
production ML models | product features | dashboards & analysis
Required skills
SAS Base, SAS/STAT, SAS Macros, CDISC standards (SDTM, ADaM), regulatory guidelines (GCP, ICH, FDA, ISO), data validation, analysis dataset development
Preferred skills
R or Python programming, CRO deliverable review, SAS macro development
Technologies
SAS, Microsoft Excel, Microsoft Word, Microsoft PowerPoint
Responsibilities
Develop complex analysis datasets and summary outputs; Create and maintain SAS programs; Perform independent program review and validation; Support ad hoc and planned analyses; Partner with Clinical Data Management and Biostatistics; Identify programming risks and data issues
Seniority
Senior, hands-on IC
