Senior Stat Programmer
Core
Lead complex clinical study programming from database integration to statistical outputs, designing advanced macros and tools while ensuring regulatory compliance.
Role type
Senior Stat Programmer (Clinical Trials)
Builds
Statistical outputs, programming specifications, and study-related deliverables for clinical trials
Domain
Life sciences / Clinical research / Healthcare intelligence
Deliverable
production ML models | product features | dashboards & analysis | client delivery
Required skills
SAS programming (Base, Graph, Macro), CDISC standards (SDTM, ADaM), clinical data understanding, statistical principles, regulatory compliance knowledge, project coordination, technical leadership
Preferred skills
R programming, ADNCA for PK analysis
Technologies
SAS, R, ADNCA
Responsibilities
Plan and oversee programming activities for complex clinical studies; Design and implement advanced macros and process improvements; Collaborate with statisticians, data managers, and clients; Mentor junior programmers; Ensure deliverables meet regulatory standards and quality benchmarks
Seniority
Senior, hands-on IC with leadership responsibilities
