Clinical statistical programmer

Job Title: Clinical Statistical Programmer (SAS / CDISC)
Location - Brazil (Remote)
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
Prepare...

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