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Tier-1 employer and metro location increase applicants, but niche SAS clinical programming reduces candidate pool.
Requires clinical trial SAS statistical programming, limiting cross-industry transferability.
Explicit 7/8 years requirement, mandatory SAS/statistical programming and clinical study experience makes filters strict.
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Lead the programming, testing, and documentation of statistical programs to create tables, figures, and listings for complex studies.
Plan and coordinate development of integrated programming solutions and database integrations from multiple studies or sources.
Manage project scope, budgets, resource forecasts and provide training and technical leadership to team members 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 and experience.
Advanced knowledge of Base SAS, SAS Graph, and SAS Macro Language required.
Knowledge of statistics, programming, and clinical drug development processes.
Work Experience Required: 7-8 years relevant experience as specified; notice period not explicitly mentioned.
Experienced in leading complex statistical programming projects, including programming, validation, and documentation.
Demonstrates capability in project management aspects such as scope, budget, and resource management for statistical programming activities.
Skilled in mentoring and providing internal consulting for technical solutions within clinical research or drug development environments.