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Title:Senior Statistical Programmer II
Location:MA - Cambridge

This position is a full time position in the Statistical Programming Department and will report to the Senior Manager of the department.

  • Be part of a growing team of experienced programmers as we continue to build our infrastructure. 
  • Be well versed in all the pertinent industry standards such as the ICH-E3 guidelines, CDISC data structures, 21 CFR Part 11 and GCP guidelines.
  • Expected to have a strong foundation in all clinical trial phases, standard reports, and familiarity with clinical data in general.
  • Expected to program efficiently in the SAS language to meet tight deadlines in an amicable work environment.

  • Have at least eight years or demonstrated high level of relevant SAS programming experience in the clinical trials industry; CRO, Pharmaceutical or Biotechnology.
  • Be well versed with the SAS modules BASE, STAT and GRAPH. The candidate is expected to utilize the SAS MACRO language for efficient and dynamic programming.
  • Bbe able to document their work suitable for internal and external audits as well as for submission purposes.
  • Be able to organize, delegate and lead a team from start to finish overseeing all production and QC functions on a project.
  • Expected to participate in internal and external technical presentations and mentor junior team members when required.
  • Distinguish themselves in an area of expertise in Statistical programming such as statistics, macros, automation etc.
  • Have strong communication and leadership skills and must be able to work independently or in team settings with little or no supervision.
  • Interact with all functional groups and be a core member of an inter-departmental team.
  • A Master’s level in Mathematics or Statistics is a plus but not required.

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