Senior SAS Programmer for Clinical Trials Full-time Job

The Senior SAS Programmer for Clinical Trials will lead the development of complex SAS programs for analyzing and reporting clinical trial data. This role requires extensive experience in SAS programming and clinical trials. Responsibilities include overseeing the creation of datasets, tables, listings, and figures, as well as ensuring data integrity and compliance with regulatory standards. You will coordinate with biostatisticians and clinical teams to meet project objectives and timelines. The role involves reviewing and validating programs, mentoring junior programmers, and contributing to the development of standard operating procedures (SOPs). Strong problem-solving skills, attention to detail, and the ability to manage multiple projects simultaneously are crucial. Knowledge of statistical analysis and regulatory submission processes is required.