SAS ProgrammerVenesco is seeking a skilled SAS Programmer to support clinical data analysis and regulatory submission activities.Key Responsibilities:Develop SAS programs for tables, listings, and figures (TLFs)Create CDISC-compliant datasets (SDTM and ADaM)Validate and document programming outputsCollaborate with statisticians and data management teamsSupport regulatory submissions and auditsMinimum Qualifications:Bachelor's or Master's degree in Statistics or related field5+ years of SAS programming experience in clinical researchExperience with CDISC standardsPreferred Qualifications:Experience supporting FDA submissionsKnowledge of Python