Clinical Statistical Programmer

Job Title: Clinical Statistical Programmer (SAS / CDISC)Location - Brazil (Remote)Role SummaryWe are seeking a detail-oriented Clinical Statistical Programmer to support clinical trial data standardization, analysis, and regulatory submissions. The ideal candidate will have strong expertise in CDISC standards (SDTM & ADaM), SAS programming, and generation of Tables, Listings, and Figures (TLFs), along with experience in quality control and submission readiness.Key ResponsibilitiesTransform raw clinical trial data into CDISC-compliant SDTM and ADaM datasetsDevelop, validate, and maintain Tables, Listings, and Figures (TLFs) for clinical study reports and regulatory submissionsWrite efficient, well-documented SAS programs for data cleaning, derivations, and reportingDevelop reusable Python or R scripts for automation, validation, and reproducible reportingPerform programming QC and peer reviews to ensure accuracy and traceabilityPrepare and maintain programming specifications, mapping documents, and annotated CRFsTroubleshoot complex data integration and derivation issuesSupport audits and regulatory inspections with reproducible code and documentationRequired QualificationsStrong experience with SAS programmingHands-on experience with CDISC standards (SDTM & ADaM)Experience generating TLFs for regulatory submissionsKnowledge of clinical trial data structures and submission processesFamiliarity with Python or R for automation (preferred)Strong attention to detail and documentation practicesPreferredExperience supporting FDA/EMA regulatory submissionsPrior experience in a Pharma, Biotech, or CRO environment