About the role

Senior Statistical Programmer at Sitero providing high-quality clinical programming outputs across various studies. Utilizing SAS programming and CDISC standards in a hybrid work environment.

Responsibilities

Create and validate edit check programs using standard validation practices
Develop SAS programs to convert data from EDC to protocol-specific SAS datasets
Review and annotate CRFs for SDTM mapping
Provide statistical programming support to generate ADaM datasets, tables, listings, and figures for individual studies
Apply advanced knowledge of CDISC standards (SDTM and ADaM) across all deliverables
Run P21 reports for both SDTM and ADaM datasets and interpret the results
Develop and validate SAS macros and format libraries
Ensure the quality of client data and data exports
Create documentation related to the generation of customer-specific SAS datasets
Maintain the SAS environment, including assistance with installation, updates, and maintenance.

Bachelor’s degree in Computer Science, Statistics, or a related field — required
8+ years of SAS programming experience in a pharmaceutical or clinical research industry environment — required
5+ years of experience working with CDISC standards, SQL, and relational databases — required
3+ years of experience with database organization and data extraction for listings and reports — required