Senior Clinical SAS Programmer

Key Responsibilities

• Developing CDISC-compliant datasets and corresponding documentation for electronic submission to regulatory agencies.
• Creating or reviewing software systems to generate displays of clinical study data as tables, listings, and graphs for electronic submission to regulatory agencies.
• Assisting statisticians by suggesting algorithms to address client analysis requests.
• Developing software validation procedures and test plans.

Requirements

• Minimum years of experience in developing software for clinical trials using the SAS system.
• Skilled in programming with SAS.
• Knowledge of additional programming languages a plus.
• Good knowledge of statistics and drug development process.
• Experience as a lead programmer for NDAs/BLAs.
• Experience overseeing the work of internal contractors and external vendors (CROs).