Extracting clinical data from a clinical data management system to generate standard and customized reports, primarily using SAS. Collaborating closely with an internal team to produce deliverables tailored to the needs of pharmaceutical and biotechnology clients. Executing analyses as specified in the protocol or the Statistical Analysis Plan (SAP), working closely with project statisticians. Programming reports and listings in response to requests from fellow project team members during ongoing studies. Establishing transfer specifications with external data source vendors. Creating SAS macros, templates, and utilities to facilitate data cleaning and reporting processes. Conducting programming tasks to transform raw clinical trial data into Study Data Tabulation Model (SDTM) format. Designing and validating global macros or systems to streamline repetitive operations and enhance programming efficiency.