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Job Title: Senior Statistical Programmer (SAS) – 7+ YearsJob Title: Principal Statistical Programmer (SAS) – 9+ YearsJob OverviewWe are looking for a Senior / Principal Statistical Programmer with strong SAS programming experience to support clinical trials (Phase 2/3 preferred). The role involves data extraction, SDTM/ADaM programming, and TLG development, ensuring high-quality, submission-ready deliverables aligned with industry standards.Key ResponsibilitiesCreate and maintain SAS programs to support clinical trial analysis and reportingDevelop analysis datasets for trial level reporting and integrated safety/efficacy activitiesProgram and QC Tables, Listings & Graphs (TLGs) as defined in SAPDevelop reusable utility macros to build a macro library supporting TLGsCollaborate with project teams to ensure timely and quality deliverablesCreate submission-ready datasets and outputs following SDLC & industry standardsMaintain project documentation as per SOPs and processesEnsure compliance with industry quality standards, guidelines, and proceduresOther duties as assignedRequired Skills & Experience7–9+ years in Pharma/Biotech/CRO or relevant consulting experienceStrong in Base SAS, Proc SQL, Macro programming, ODSStrong experience with CDISC standards: SDTM & ADaMExperience in clinical trial phases 1–4 (Phase 2/3 preferred)TLG programming, QC/validation as per SAPKnowledge of ICH/GCP, 21 CFR Part 11Knowledge of coding dictionaries: MedDRA, WHO, ICD-9, COSTARTStrong communication, multitasking, and documentation skillsGood to HaveNDA submission experiencePooled data analysis experienceSAS modules: SAS/STAT, SAS/GRAPH, SAS/Connect, SAS/AccessShell/batch scripting exposureEducationBachelor’s in Science / Computer Science / related field (Master’s preferred)