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A company is looking for a SAS Programmer. Key Responsibilities Provide comprehensive programming support for clinical trials, including development of programs and analysis datasets Manage and deliver assignments with quality and within timelines, ensuring compliance with regulatory requirements Standardize deliverables across study projects and communicate programming deliverables' status and resource gaps Required Qualifications Bachelor's or Master's Degree in Science, Statistics, Information Technology or equivalent 7+ years of professional experience in a pharmaceutical or clinical research setting as a programmer Proficient knowledge of clinical trials, drug development processes, and statistical concepts Strong understanding of SDTM and ADaM standards Demonstrated proficiency in using SAS for analysis datasets and TLGs