Sr. Clinical Sas Programmer Analyst, BS., deg., in Phar., or Stat., w/ 1 yr., of exp; Wrk., on SDTM, TFL & ADAM Spec., Run spec., compliance test, Edit & CDISC Validator checks.
Wrk., w/ data science & R-prog., to produce graphs for adverse events, vital signs & lab domains.
Use SAS ODS Graphic tools to create graphs for placebo controlled studies.
Exp., in CDISC SDTM, ADaM, SAS export files, Data anal., interpretation of clinical trial data, Base, Macros, STAT, Graph, SQL & SAS/ODS.
Wrk., on cleaning, extraction, programing study, Data Management, Data validation plan.
Generate TLFs, validation data, reports, & maintenance of study doc., 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
Location/Region: King Of Prussia, PA (US - 19406)