Senior SAS Developer

Role: Senior SAS developer supporting clinical data automation within a regulated life sciences environment, primarily focusing on clinical trial data standardization, validation, and automation. Responsibilities: develop, validate, and maintain SAS-based programming for SDTM, ADaM, Define.xml, Reviewer’s Guides, and submission packages; design automated workflows for data ingestion, validation, and reporting; build reusable macros and utilities; collaborate cross-functionally to convert manual processes into scalable automated solutions; support integration with P21 systems and metadata repositories. Requirements: B.Sc./M.Sc. in Biostatistics, Bioinformatics, or related field; minimum 6 years of experience in SAS programming for clinical trials; expertise in CDISC standards, Pinnacle 21 validation, and regulatory submission standards; proficiency in SAS, R, and/or Python; strong understanding of clinical trial data structures and standards. Preferred: experience with R or Python, metadata-driven programming, API/workflow integration, and clinical data automation. High-Value: expertise in SDTM, ADaM, Pinnacle 21, validation processes, and automation tools for clinical trial data management and regulatory submissions. Work setup: not specified but implies a regulated, collaborative environment.