Catalyst Clinical Research is hiring a
Principal Statistical Programmer

Summary

The job is for a Senior Statistical Programmer in the Clinical Development Operations team. Responsibilities include creating safety and efficacy SAS datasets, performing data checks, QC/validation of datasets, maintaining professional relationships, ensuring data analysis quality, and contributing to functional-level standards. Required qualifications are a Bachelor's Degree in Computer Science/Mathematics or equivalent, with a preferred Master's degree, 5 years of SAS programming experience, hands-on CDISC/SDTM/ADaM programming experience, and previous experience in a pharmaceutical research or CRO setting.

Responsibilities

• Creation of safety and efficacy SAS datasets
• Creation of project specific macros and formats
• Performing data checks as needed, to ensure integrity and correctness of data displays and to understand structure and content of data
• Perform QC/validation of datasets, tables, listings, figures to verify the output
• Establish, maintain, and strengthen a professional working relationship with clients, potential clients, regulatory agencies, collaborating staff, vendor, and subcontract personnel
• Represent department and company in a multi-disciplinary setting, including project team meetings, client meetings/presentations
• Ensure the quality and integrity of data analysis and reporting
• Maintain awareness of project budgets and tasks, and effectively communicate the status of such tasks to management
• Contribute to the development of functional-level standards, tools, and templates
• Interact across operational areas as required
• Interact with sponsor representatives as required