WHAT YOU'LL DO

• Perform data manipulation, analysis and reporting of clinical trial data;
• Develop and maintain department / system-level macros
• Create/review SDTM and ADaM specifications
• Create/validate SDTM data sets;
• Create/validate analysis data sets;
• Create/validate patient profiles
• Program and generate tables, figures and listings (TFLs);
• Validate and document SAS programs and output;
• Fulfill ad-hoc analysis requests;
• Other services as identified by Vir Biotechnology.

WHO YOU ARE AND WHAT YOU BRING

• Bachelor’s degree or higher, preferably in a scientific discipline such as Statistics, Mathematics, Computer Science, or related applicable field;
• Minimum of ten (10) years’ SAS programming experience in the pharmaceutical/biotech industry with extensive experience using CDISC standards;
• Create source and validation programs using SAS software for SDTM datasets, ADaM datasets, and tables, figures and listings (TFLs) 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/GTL;
• Proficient in Microsoft Word, Excel, and PowerPoint.