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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.

The Principal Statistical Programmer oversees clinical trial programming, implementing reporting and analysis for pharmaceutical clients while ensuring quality and regulatory compliance.

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.

The Senior Statistical Programmer will conduct data manipulation, analysis, and reporting for clinical trials using SAS. This role involves generating SDTM/ADaM datasets, performing QC, and leading project tasks while collaborating with cross-functional teams.

The Senior Statistical Programmer will manage clinical trial data using advanced SAS skills, ensuring quality through data analysis, manipulation, and reporting, while adhering to CDISC standards and collaborating with cross-functional teams.

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

The Principal Statistical Programmer oversees programming activities for clinical trials, ensuring high-quality data summaries and compliance with statistical standards while mentoring CRO programmers.

The Principal Statistical Programmer will generate CDISC datasets, develop SAS and R programs, oversee CRO deliverables, and ensure high-quality statistical analysis for clinical trials.