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 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 Interested candidates please share your profiles to