Principal Statistical Programmer
Core
Implement statistical analysis plans and provide QC'd data packages (tables, figures, listings) for publications and ad-hoc analysis requests.
Role type
Principal Statistical Programmer
Builds
Clinical trial data outputs, tables, figures, and listings for medical publications
Domain
Clinical research / Biostatistics / Pharmaceutical R&D
Deliverable
production ML models | product features | dashboards & analysis | research
Required skills
SAS programming, SDTM & ADaM (CDISC) standards, post-hoc statistical analysis, statistical analysis plan implementation, data package documentation, macro development
Preferred skills
Advanced programming methods, mentorship of new team members
Technologies
SAS
Responsibilities
Develop and maintain relationships with Medical Affairs stakeholders and local/global biostatistics teams; Coach and mentor new team members; Conduct post-hoc statistical analyses of clinical trial data; Design, develop, test, implement, and document statistical programming; Produce well-documented data packages including tables, listings, and figures; Ensure SOPs are followed and timelines/quality are met
Seniority
Principal, hands-on IC with mentorship responsibilities
