Senior SAS Programmer / Biostatistician - Seneca Holdings, LLC

Key Responsibilities

• Develop, validate, and maintain complex SAS programs for clinical trial data analysis and reporting.
• Design and implement SAS macros and reusable code libraries to streamline analysis workflows.
• Collaborate with biostatisticians, data managers, and project teams to translate statistical protocols into executable SAS code.
• Perform data quality checks, debugging, and performance optimization of SAS programs.
• Document code, procedures, and analysis outputs in compliance with regulatory standards (FDA, EMA, etc.).

Requirements

• 5+ years of experience in SAS programming within clinical research or public health environments.
• Strong knowledge of SAS/STAT, SAS Macro language, and data step programming.
• Proficiency in biostatistical concepts, study design, and regulatory reporting.
• Excellent problem‑solving skills and attention to detail.
• Effective communication skills for cross‑functional collaboration.