Principal Programmer Single Sponsor

1 month ago


Riyadh, Saudi Arabia Fortrea Full time
  • Ideally you will have knowledge in all aspects of clinical trials, from initial study set-up to study completion, with an understanding of the roles and responsibilities of all related disciplines, e.g. Biostatistics and Clinical Data Management
  • Expert knowledge of base SAS, SAS macros, SAS/STAT and in debugging SAS programs
  • Broad knowledge of all CDISC requirements related to SDTM and ADaM, including define.xml, Reviewer's Guides and submission standards
  • An autonomous, collaborative work style, a curious mind and a keen attention to detail


  • Riyadh, Saudi Arabia Fortrea Full time

    As a Senior Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex clinical trials (phases I-III) for renowned, innovative and global top pharmaceutical companies. Oftentimes you will have the opportunity to lead studies through various phases of the clinical development plan...


  • Riyadh, Ar Riyāḑ, Saudi Arabia Fortrea Full time

    As a Senior Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex clinical trials (phases I-III) for renowned, innovative and global top pharmaceutical companies. Oftentimes you will have the opportunity to lead studies through various phases of the clinical development plan...


  • Riyadh, Ar Riyāḑ, Saudi Arabia Fortrea Full time

    Ideally you will have knowledge in all aspects of clinical trials, from initial study set-up to study completion, with an understanding of the roles and responsibilities of all related disciplines, e.g. Biostatistics and Clinical Data ManagementExpert knowledge of base SAS, SAS macros, SAS/STAT and in debugging SAS programsBroad knowledge of all CDISC...


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