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The Clinical Data Engineer serves as an expert in USDM, driving digital protocol generation and enabling seamless data flow across the clinical development lifecycle, while collaborating across functions to optimize processes and ensure compliance with industry standards.

The Senior Clinical Data Manager oversees data management tasks from study initiation to database lock, ensuring high-quality data delivery, adherence to timelines and budgets, and leading project activities with minimal supervision. Responsibilities include user acceptance testing, data cleaning, project documentation, training staff, and managing client communication.

The Senior Statistical Programmer will support and lead clinical trials by performing data manipulation, analysis, and reporting using SAS programming. Responsibilities include generating SDTM and ADaM datasets, validating programming, creating reports, and collaborating with cross-functional teams.

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.