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This role provides technical support in clinical programming, leads projects, mentors staff, and ensures quality deliverables while managing multiple studies.

The Senior Statistical Programmer designs and implements programs for statistical analysis, manages project documentation, oversees programming tasks, and ensures outputs meet quality standards in a clinical setting.

The Senior Clinical Programmer develops and maintains Python scripts for clinical data, interprets SAS programs, collaborates with teams, and ensures accurate data handling and compliance.

The Stat Programmer II will analyze clinical data using SAS and R, ensure compliance with quality standards, and collaborate with teams while managing multiple projects and timelines.

The Senior/Principal Statistical Programmer develops programming code for statistical analysis, ensures output quality, manages project documentation, and leads programming activities while mentoring junior staff.

The Senior Principal Statistical Programmer will be responsible for analyzing clinical data, programming statistical analyses, and contributing to clinical trials, ensuring compliance and quality throughout the process.

Lead statistical programming activities, develop programming code using SAS, ensure quality standards, manage multiple projects, and mentor junior staff.

Manage regulatory strategies and lifecycle for global products, oversee project teams, mentor staff, and provide regulatory guidance while ensuring compliance and quality.

Lead software development and deployment in R and Python, manage CI/CD pipelines, oversee data strategy, and enhance performance optimization.

The Sr Biostatistician-RWE will manage statistical activities, develop SAP, oversee CSR reviews, and support clinical trials using R and SAS with expertise in RWE studies and CDISC standards.