Business Analysts. Multiple openings. Work on various phases of the clinical trial process and develop data tables, listings, and graphs. Validate and ensure quality of displays and datasets per QC levels for clinical and pharmaceutical trials. Write high level design documents and perform data analysis. Convert Legacy to CDISC standards and write SDTM specifications. Develop analysis datasets and programs to generate reports and validate SAS. Work with demography, adverse event, vital signs, ECG, medication, and lab data. Act as POC for pharmaceutical clients and ensure deliverables. Use SAS/ODS to deliver outputs, implement clinical trial data standards, and develop ad-hoc requests. Work with SAS, RTF, and Excel. 40 hrs/wk. Must have Master's degree or equivalent in Computer Science, Electr Engineering, Biology, Biotechnology, or a related field (will accept a Bachelor's degree plus 5 years of progressive post baccalaureate experience in lieu of a Master's) and 1 year experience (or 1 year experience as a Clinical SAS Programmer, or related occupation). Must have 1 year experience writing high level design documents, performing data analysis, and working with SAS.