Job Description

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 & 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 programm...

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