STATISTICAL PROGRAMMERS

Perform all aspects of data management, statistical programming, analysis & reporting of clinical trials’ data deliverables. Generate tables, listings, and graphs using Base SAS, SAS Macros, SAS PROCS, SAS SQL and SAS ODS. Develop and implement standards for SDTM implementation. Perform data validation, discrepancy management, data extraction, and database lock. Develop SAS programs to map data into SDTM domains and derive safety Analysis Data Model (ADaM) datasets. Prepare ad hoc reports. Associates Degree in Science, Technology, or Engineering (any) along with 2 years of experience in job offered or related occupation is required. Work location: North Brunswick, NJ and various unanticipated locations throughout the U.S.Send Resume to HR Dept., Aptiva Corp., 825 Georges Road, Suite 1, North Brunswick, NJ 08902.