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The Principal Statistical Programmer provides technical leadership in SAS and R programming for clinical trial data analysis, reporting, and regulatory submissions, ensuring compliance and quality control while managing teams and resources.

The Principal Statistical Programmer leads SAS and R programming for clinical trials, ensuring compliance, quality, and effective communication with stakeholders.

The Senior Statistical Programmer will manage and report on clinical trial data, generating SDTM/ADaM datasets and collaborating with cross-functional teams in a pharmaceutical setting.

As a Senior Statistical Programmer, you will perform data manipulation and analysis for clinical trials, generate SDTM and ADaM datasets, ensure quality control, and communicate with project teams while potentially leading multiple projects.

The Senior Statistical Programmer will use advanced SAS skills to support Phase I-IV clinical trials, generate datasets, and lead data analyses.

Lead statistical activities for clinical trials, collaborate with stakeholders, oversee programming and junior statisticians, and apply statistical methods for data analysis.