Senior Statistical Programmer (Permanent role)
Core
Lead statistical programming activities for clinical trials, delivering derived datasets, tables, figures, and listings for pharmaceutical and biotech clients.
Role type
Senior Statistical Programmer (Clinical Trials)
Builds
CDISC-compliant electronic submissions, statistical analysis plans, and derived datasets for clinical trials.
Domain
Pharmaceutical/Biotechnology Clinical Development
Deliverable
production ML models | product features | dashboards & analysis
Required skills
SAS programming, SAS Macro language, R programming, CDISC standards (SDTM/ADaM), data integration (ISS/ISE), statistical analysis plan design
Preferred skills
Drug development process knowledge, ad hoc exploratory analysis, vendor management
Technologies
SAS, R
Responsibilities
Program and validate derived datasets, tables, figures, and listings; oversee programming deliverables from CROs; contribute to design of Case Report Forms and Statistical Analysis Plans; ensure on-time, high-quality delivery of programming artifacts.
Seniority
Senior, hands-on IC