Full job description Roles & Responsibilities: Bachelor's degree or equivalent, preferably in a scientific discipline such as Statistics, Mathematics, Computer Science, or related applicable field. Minimum of 5 to 8 years' SAS programming experience in the pharmaceutical/biotech industry with some experience using CDISC standards. Create source and validation programs using SAS software for SDTM datasets, analysis datasets, and tables, listings, and graphs (TLGs) for multiple studies/products. Integrates data across multiple studies or drug programs. Expertise in the development and use of system-level macro programs. Experience in programming using SAS/GRAPH. Proficient in Microsoft Word, Excel, and PowerPoint. Perform data manipulation, analysis and reporting of primarily clinical trial data. Create SDTM data sets. Create analysis data sets. Program and generate tables, listings and graphs (TLGs). Validate and document SAS programs and output. Fulfill ad-hoc analysis requests.