Sr. Scientist, Stat. Programming - Late-Stage (Non-Oncology) (Hybrid)
Core
Design and maintain statistical datasets and execute analysis/reporting deliverables (tables, listings, figures) for late-stage drug and vaccine clinical development projects.
Role type
Senior Statistical Programmer (Late-Stage Clinical)
Builds
Safety and efficacy analysis datasets, regulatory submission deliverables, and post-marketing support materials.
Domain
Life Sciences / Clinical Trials / Biostatistics
Deliverable
production ML models | product features | dashboards & analysis
Required skills
SAS programming (data steps, procedures, macros, graphs), CDISC ADaM standards, clinical trial programming, statistical database design, project planning, global team coordination
Preferred skills
R programming, Python, regulatory submission experience, mentoring programmers, process improvement
Technologies
SAS, Microsoft Project, R, Python
Responsibilities
Develop and validate statistical analysis and reporting deliverables; design and maintain statistical datasets; coordinate global programming teams including outsource providers; manage project plans and resource forecasting; serve as statistical programming point of contact.
Seniority
Senior, hands-on IC with project leadership
