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Senior Statistical Programmer II responsible for SAS programming tasks in clinical trial analysis and reporting. Works closely with Biostatistics and Data Management departments, leads programming assignments, develops standard macros, and ensures quality and accuracy of work.

The Tableau Developer is responsible for developing complex data analysis, methodologies, and predictive data models for assessing clinical trial outcomes. They coordinate data collection, build interactive dashboards in Tableau, create visually striking graphics, and lead multiple complex projects. The role requires 5-8 years of Product Development experience in Tableau Desktop and SQL Server.

The Statistical Programmer II is responsible for performing SAS programming tasks for clinical trial analysis and reporting, working closely with the Biostatistics and Data Management departments on various clinical projects.

The Principal Statistical Programmer at Precision Medicine Group plays a key role in performing SAS programming tasks required for clinical trial analysis and reporting. Responsibilities include leading programming assignments, providing mentorship, staying informed of industry developments, developing standard macros, and ensuring quality and accuracy of work. Qualifications include a Bachelor's degree and at least six years of experience as an SAS programmer in clinical trials.