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The Senior Statistical Programmer will utilize advanced SAS skills for data manipulation, analysis, and reporting in clinical trials, while leading multiple projects and ensuring adherence to CDISC standards.

The Senior Statistical Programmer will conduct data analysis and reporting for clinical trials, generate SDTM and ADaM datasets, and communicate with cross-functional teams while leading projects.

The Senior Clinical Data Manager oversees comprehensive data management activities throughout the clinical trial process, ensuring compliance and quality of data. The role includes collaboration with stakeholders, handling regulatory submissions, and managing multiple drug development programs.

The Principal Statistical Programmer will generate specifications and datasets, develop and validate SAS/R programs, oversee CRO deliverables, and ensure compliance with regulations for clinical studies.

The Principal R Shiny Developer will create and maintain interactive Shiny applications, optimize code, develop Microsoft Power Apps solutions, and ensure documentation quality.

The Executive Consultant will lead strategic consulting in Quantitative Clinical Pharmacology, mentor teams, and engage with clients for business development and scientific expertise.

Lead clinical studies by providing statistical support, employing advanced analytical methods, and collaborating with cross-functional teams to optimize clinical development processes.

The Senior Clinical Data Manager oversees clinical data management from study start-up to database lock, ensuring compliance and quality in deliverables across multiple CROs. Responsibilities include vendor oversight, risk mitigation, regulatory submissions, and managing budgets and timelines for data management activities.