Responsibilities: Experience supporting programmers within a study team for the creation and QC of analysis datasets, TFLs, or standard tools following CLIENT standard data models or user requirements. pplication of standard tools developed for the study or project, as well as participation in the development of new standards and tools. dherence to company SOPs and guidelines in creating programming deliverables. Compliance with procedures for the retention of data, records, and information in clinical studies. Requirements: Proficiency in SAS (Base, Stat, Macro, Graph). MS (BS) in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline. 5-7 years of programming experience, preferably in processing clinical trial data in the biotechnology, pharmaceutical, or health-related industry. SAS Certification is a plus. Experience in SAS programming, especially in a clinical data environment. Exposure to relational database structure. Understanding of reporting systems. Experience with implementing standardization methodology. Demonstrated teamwork and interpersonal skills, with strong verbal and written communication abilities in a global environment. bility to support study requirements within challenging timelines under the direct supervision of the programming lead. Katalyst Healthcares and Life Sciences
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