Senior SAS Developer

Role: Senior SAS developer supporting Clinical Data Automation within biopharma clinical trial environments. Objectives include developing, validating, and maintaining automated workflows for clinical data standardization, validation, and submission-readiness. Responsibilities encompass designing data pipelines for SDTM, ADaM, and Define.xml, applying CDISC standards, and integrating with P21 systems; building reusable automation utilities; and collaborating cross-functionally to optimize data processes. Requirements: B.Sc./M.Sc. in Biostatistics, Bioinformatics, or related; 6+ years in clinical programming for drug development; extensive experience with SAS, CDISC standards, Pinnacle 21, and clinical trial data structures; familiarity with R or Python is a plus; strong communication skills. HighValue: expertise in clinical data validation, automated data flow design, regulatory submission standards, and metadata-driven programming. WorkSetup: not specified, but likely in a regulated, collaborative clinical environment.