Sr. Programmer Analyst
Bachelor of Science degree in Computer Science, or Electrical & Communication Engineering & 5 years’ of experience: Plan & coordinate programming, testing & document of statistic, program; Generate tables, listings & graphs using SAS Base/Macros/Graph/SQL. Perfect analysis of clinical trial data for Phase I, II & III clinical studies. Perfect 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.
We are an Equal Employment Opportunity (EEO) employer and does not discriminate on the basis of race, color, national origin, religion, gender, age, veteran status, political affiliation, sexual orientation, marital status or disability (in compliance with the Americans with Disabilities Act) with respect to employment opportunities.
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