Clinical Statistical Programmer (SAS / CDISC)

Job Title: Clinical Statistical Programmer (SAS / CDISC) Location - Brazil Role 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 specification...