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Tier-1 brand, metro location, and mid-level generalist role increase competition.
Clinical SAS/statistical programming is specialized to pharma/CRO, limiting cross-industry transferability.
Explicit 7–8 year requirement and mandatory SAS skills tighten filters.
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Lead the programming, testing, and documentation of statistical programs for complex studies, including tables, figures, listings, and analysis datasets.
Plan and coordinate integration of databases from multiple studies and develop programming documentation for complex projects.
Manage project scope, budgets, and resources; provide advanced technical expertise and training to junior staff; act as statistical team lead for single or multiple complex studies.
Master's degree in Computer Science or related field with 7 years relevant experience OR Bachelor's degree with 8 years relevant experience OR equivalent combination of education, training, and experience.
Advanced knowledge of Base SAS, SAS Graph, and SAS Macro Language.
Knowledge of statistics, programming, and clinical drug development process.
Work Experience Required: 7-8 years depending on degree, as specified.
Experienced in managing complex statistical programming projects, including budget and scope management at the project or group level.
Proficient in advanced SAS programming with ability to develop, implement, and validate new process technologies and macros.
Able to provide technical leadership and training within teams, and to collaborate with internal and external clients for solution delivery in clinical drug development contexts.