Statistical Programmer Analyst I/II -Permanent Role- Hybrid (2 days a week)
Core
Develop, validate, and maintain statistical programs using SAS and R for clinical trial data analysis, reporting, and regulatory submissions.
Role type
Statistical Programmer Analyst
Builds
Tables, Listings, and Figures (TLFs) for clinical studies
Domain
Pharmaceutical/Biotechnology clinical trials
Deliverable
production ML models | product features | dashboards & analysis
Required skills
SAS programming, R programming, CDISC standards (SDTM, ADaM), clinical trial data knowledge, regulatory compliance, data manipulation, quality control
Preferred skills
FSP model experience, FDA/EMA submission exposure, global pharmaceutical client experience
Technologies
SAS, R
Responsibilities
Develop and validate statistical programs for TLFs, perform data manipulation and visualization, collaborate with biostatisticians and data management teams, conduct QC of programming outputs, support submission activities and documentation
Seniority
Mid-level, hands-on IC