SAS Programmer Analyst

BS degree in Pharmaceutical or Statistics with 1 year of experience; Work on SDTM, TFL & ADAM Specifications, Run specifications, compliance test, Edit & CDISC Validator checks. Work with data science & R-program to produce graphs for adverse events, vital signs & lab domains. Use SAS ODS Graphic tools to create graphs for placebo controlled studies. Experience in CDISC SDTM, ADaM, SAS export files, Data analysis, interpretation of clinical trial data, Base, Macros, STAT, Graph, SQL & SAS/ ODS. Work on cleaning, extraction, programming study, Data Management, Data validation plan. Generate TLFs, validation data, reports, & maintenance of study documents, Must be willing to travel and/or relocate to work in unanticipated locations throughout the US.