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Title:Senior Statistical Programmer I
Location:MA - Cambridge

The candidate is expected to program efficiently in the SAS language to meet tight deadlines in an amicable work environment and will report to the Director of the department.

  • Be part of a growing team of experienced programmers as we continue to build our infrastructure.
  • Expected to 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.
  • Have a strong foundation in all clinical trial phases, standard reports, and familiarity with clinical data in general.
  • Utilize the SAS MACRO language for efficient and dynamic programming. 
  • Document their work suitable for internal and external audits as well as for submission purposes. 
  • Organize and lead a team from start to finish overseeing all production and QC functions on a project.
  • Participate in internal and external technical presentations and mentor junior team members when required.
  • Interact with all functional groups and be a core member of an inter-departmental team.

  • The candidate should have at least five years or demonstrated high level of relevant SAS programming experience in the clinical trials industry; CRO, Pharmaceutical or Biotechnology.
  • The candidate should be well versed with the SAS modules BASE, STAT and GRAPH.
  • The candidate should have strong communication and leadership skills and must be able to work independently or in team settings with little or no supervision.  
  • A Master's level in Mathematics or Statistics is a plus but not required.

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