Sr. SAS Programmer, MS., deg., in CS., or Info., Sys., Tech., w/ 2 yrs., of exp.,Prepare SDTM & ADAM Spcf., Wrk w/ compliance test, CDISC Validator checks & resolving issues. Wrk SDTM/ADAM/TFL. Prf., adverse events data visualization using SAS graphs. Create Define.xml (Case Report Tabu., Data Defi., Spec.,), Therapeutic specific SDTM (TU,TR & RS - oncology) & ADaM (ADTU,ADTR - oncology ) data sets .Prepare ISS & ISE reports. Des., & impl., clinical data reporting process for new drug (NDA) or biological (BLA). Rev., & prf., quality checks on clinical trial data. Cond., interim anal., esub wrk., for developed datasets for regulatory submissions, Map Legacy data in SDTM format. Create analysis datasets based on ADaM 2.1 std., Dev., Ad-hoc tables, figures & listings. Must be willing to travel and/or relocate to work in unanticipated locations throughout the US. Send Resume to PVR Technologies, 144 E Dekalb Pike, Suite 100, King of Prussia, PA, 19406.