Sr. Scientist, Stat. Programming, Late-Stage Oncology (Hybrid)
Core
Statistical programming for late-stage clinical trials of drugs and vaccines, ensuring data integrity for regulatory submissions and safety/efficacy analysis.
Role type
Senior Statistical Programmer (Clinical Trials)
Builds
Statistical analysis datasets, tables, listings, figures, and regulatory submission deliverables for global clinical development projects.
Domain
Biopharmaceuticals / Oncology / Clinical Data Management
Deliverable
production ML models | product features | dashboards & analysis
Required skills
SAS programming (data steps, procedures, macros, graph), CDISC standards, ADaM standards, database management, clinical trial programming, statistical analysis, project leadership, strategic thinking
Preferred skills
Python, R, R Shiny, GenAI tools, regulatory submission experience, mentoring, process improvement
Technologies
SAS, Microsoft Project, Python, R, R Shiny
Responsibilities
Design and maintain statistical datasets for clinical development; develop and validate analysis/reporting deliverables; lead global programming teams including outsource providers; ensure compliance with SOPs and industry standards; anticipate stakeholder requirements for analysis plans.
Seniority
Senior, hands-on IC with leadership responsibilities
