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Strong employer brand and metro location but niche SAS clinical programming reduces applicant density.
High because clinical SAS statistical programming skills are specialized to pharmaceutical and CRO settings.
High due to explicit years, degree options, and mandatory SAS/statistics technical requirements.
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Lead and coordinate programming, testing, and documentation of statistical programs and analysis databases for complex clinical studies.
Provide technical expertise and internal consulting to develop integrated programming solutions and process methodologies for the department.
Manage scope, budgeting, and resource forecasts for single complex studies; act 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 experience OR equivalent education/training.
Advanced knowledge of Base SAS, SAS Graph, and SAS Macro Language.
Knowledge of statistics, programming, and clinical drug development processes.
Work Experience Required: Minimum 3-4 years in relevant statistical programming roles.
Experienced in handling complex clinical study data programming and integration across multiple studies or sources.
Capable of independently providing advanced technical solutions and managing project scope and budgets.
Demonstrates leadership in coordinating teams, developing new processes, and training junior programmers within clinical research environments.