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Title:Contract Remote SAS Programmer
Location:US - Anywhere

Be able to communicate effectively within a multi-disciplinary project team, and to effectively organize and manage multiple assignments with tight timelines

  • Experience of creating and validating large complex integrated clinical trial data in CDISC format (SDTM / ADaM) with knowledge of clinical trial data management
  • Experience creating and validating tables, listings, graphs using SAS/BASE, SAS/STAT, SAS/Macro, SAS/SQL, and SAS/GRAPH; use of S-Plus for graphs is a plus
  • Evidence of initiative and motivation, strict attention to detail, and excellent problem solving skills

  • 4+ years of pharmaceutical experience on clinical trial data processing, analysis and reports, working on ISS (integrated Safety Studies) is a plus

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