Associate Principal Scientist, Stat. Programming - A&R Standards, Innovation (Hybrid)
Core
Design, develop, and deliver efficient, flexible, and modular analysis and reporting standards for drug and vaccine projects across all therapeutic areas.
Role type
Associate Principal Scientist, Statistical Programming
Builds
Global programming standards for ADaM datasets, efficacy analysis, and safety analysis
Domain
Biopharmaceutical R&D / Clinical Data Standards
Deliverable
production ML models | product features | dashboards & analysis
Required skills
SAS programming (data steps, procedures, macros, graph), CDISC SDTM/ADaM standards, clinical trial programming, statistical concepts, data management, project management, technical consultation
Preferred skills
R, Python, XML, Unix/Linux environment, complex analysis plan implementation, natural language processing
Technologies
SAS, R, Python, XML, Unix/Linux
Responsibilities
Develop and validate global programming standards for ADaM, efficacy, and safety analysis; Design and develop complex programming algorithms; Provide technical consultation to statistical programmers and statisticians; Represent company on industry initiatives (R Consortium, TransCelerate, PHUSE, CDISC); Collaborate with stakeholders to drive Analysis & Reporting standard programs
Seniority
Senior, hands-on IC with program-level leadership
