Associate Principal Scientist, Statistical Programming
Core
Develop statistical programming analysis and reporting deliverables for global stakeholders in clinical trials, transforming data into analysis datasets and creating tables/figures per analysis plans.
Role type
Associate Principal Scientist, Statistical Programming
Builds
Statistical programming deliverables (tables, figures, datasets) for clinical trial efficacy and safety analyses
Domain
Clinical Trials / Biopharmaceuticals / Oncology
Deliverable
production ML models | product features | dashboards & analysis
Required skills
SAS programming (data steps, procedures, macros, graph), CDISC SDTM/ADaM standards, eSubmission package preparation (ADRG, XPT, Pinnacle 21), large database manipulation, oncology therapeutic area concepts, pharmacokinetic data analysis
Preferred skills
R programming, leading study programming deliverables for multiple studies
Technologies
SAS, R, Pinnacle 21, XPT, ADRG
Responsibilities
Gather and interpret user requirements for analysis and programming requests, retrieve and transform data into analysis datasets, write custom statistical programs not available in commercial software, partner with stakeholders to reduce programming tasks and increase efficiency
Seniority
Senior, hands-on IC
