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Tier-1 employer and common clinical SAS role attract moderate competition despite niche SAS requirement.
Clinical SAS programming strongly favors pharma/clinical-trials backgrounds, limiting cross-industry portability.
Explicit 1–2 year experience bands plus mandatory SAS and statistics skills increase shortlisting strictness.
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Develop, test, and document statistical programming solutions for creating tables, figures, listings, and analysis datasets.
Plan and lead programming tasks including database integration and quality control for clinical studies, potentially acting as statistical team lead for single studies.
Manage scope of work, estimate project progress, handle out-of-scope tasks, and may manage budget, resources, and forecasting for individual studies.
Master's degree in Computer Science or related field with 1 year relevant experience, OR Bachelor's degree with 2 years relevant experience.
Proficient in Base SAS, SAS/STAT, and SAS Macro Language for statistical programming.
Knowledge of statistics and clinical drug development process.
Work Experience Required: 1-2 years relevant statistical programming experience.
Experienced in leading statistical programming projects with responsibility for scope and resource management at study level.
Strong technical expertise in SAS programming and clinical data integration across multiple studies.
Capable of providing technical guidance and training to junior staff and collaborating with internal and external stakeholders to deliver project solutions.