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As a TMF Specialist II, you will manage trial master file documents, ensure compliance with guidelines, perform quality checks, and support documentation activities while collaborating with teams to resolve issues and maintain TMF effectiveness.

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.

The Sr Statistical Programmer develops and maintains programs for analysis datasets, provides statistical programming support, ensures data integrity, collaborates with stakeholders, and directs lower-level professionals while managing programming processes.

The role involves advanced R programming and Shiny development, focusing on web technologies, data integration, visualization, and performance optimization while supporting agile methodologies.

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