Sr. Programmer Analyst
Sr. Programmer Analyst
BS degree in Computer Science or Electronics & Communication, Engineering & 5 years' of experience; Plan & coordinate programming, testing & documentation of stat., program; Generate tables, listings & graphs using SAS Base/Macros/Graph /SQL. Perform analysis of clinical trial data for Phase I, II & III clinical studies. Perform data cleansing & create Ad-hoc reports. Generate reports using Proc-report. Produce RTF, MSWord, PDF & HTML formatting files using SAS/ODS. Experience in QC of CDISC SDTM datasets. Develop & enhance of SAS program, Create various safety tables (Summary of Demographics, Adverse Events, Maximum severity grade, Lab Shift tables. Develop utility macros for several clinical studies & create tables using Macros. Transform data in various formats (Excel, CSV, Oracle database) into SAS datasets. Must be willing to travel and/or relocate to work in unanticipated locations throughout the US.