Role :: Clinical Statistical Programmer (SAS / CDISC) Location :: Brazil/Remote Duration :: Long Term ContractRole Summary We 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 Responsibilities • Transform raw clinical trial data into CDISC-compliant SDTM and ADaM datasets • Develop, validate, and maintain Tables, Listings, and Figures (TLFs) for clinical study reports and regulatory submissions • Write efficient, well-documented SAS programs for data cleaning, derivations, and reporting • Develop reusable Python or R scripts for automation, validation, and reproducible reporting • Perform programming QC and peer reviews to ensure accuracy and traceability • Prepare and maintain programming specifications, mapping documents, and annotated CRFs • Troubleshoot complex data integration and derivation issues • Support audits and regulatory inspections with reproducible code and documentation Required Qualifications • Strong experience with SAS programming • Hands-on experience with CDISC standards (SDTM & ADaM) • Experience generating TLFs for regulatory submissions • Knowledge of clinical trial data structures and submission processes • Familiarity with Python or R for automation (preferred) • Strong attention to detail and documentation practices Preferred • Experience supporting FDA/EMA regulatory submissions • Prior experience in a Pharma, Biotech, or CRO environment