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 & ADa M), 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 ADa M 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
· Prep...