SAS Clinical Programmer

  Our client has immediate opening for Contract SAS Programmerwho will be responsible for planning, writing and executing statistical programs designed to analyze clinical trial data. Additionally, you will assess data accuracy and consistency, identify protocol violations, implement statistical analyses, design and develop analysis files and produce tables, figures and listings; represent department on cross-disciplinary teams; participate in the development of Case Report Forms and Quality Control Specifications; and the design of standard dataset structures and software. This is a deadline driven high output environment, additional hours may be necessary to meet commitmentsREQUIREMENTS: -  Must have CDISC SDTM experience is required - specifically Mapping Data from Legacy format to CDISC SDTM standards. -  Previous experience in the production of either Integrated Efficacy or Integrated Safety analysis across multiple studies is preferred. -  Must have familiarity with common statistical analyses and extensive knowledge of SAS and other software packages used to perform statistical analyses.     RemX IT Staffing is an Equal Opportunity Employer