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Strong employer brand, metro location, and mid-level experience increase applicant competition.
Role demands clinical SAS statistical programming expertise, limiting cross-industry portability.
Explicit years requirement plus mandatory SAS and clinical domain expertise make shortlisting stringent.
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Lead programming, testing, and documentation of statistical programs for complex studies including creation of statistical tables, figures, and listings.
Plan and coordinate development of integrated programming solutions and databases from multiple studies to meet client needs.
Manage project scope, budget, resources, and forecasts for single complex studies; serve as statistical team lead and provide training to junior staff.
Master's degree in Computer Science or related field with 3 years relevant experience, or Bachelor's degree with 4 years relevant experience, or equivalent combination of education and experience.
Advanced knowledge of Base SAS, SAS Graph, and SAS Macro Language required.
Knowledge of statistics, programming, and clinical drug development process required.
Work Experience Required: Minimum 3-4 years relevant experience depending on education level.
Experienced in managing complex statistical programming projects including budgeting and resource planning.
Skilled in developing and validating new process technologies, macros, and applications within clinical research context.
Demonstrates leadership capacity through training and guiding junior staff and serving as technical expert for internal and external clients.