The Senior SAS Programmer is responsible for the development of SAS program and macro utilities pertaining to clinical trials

Main responsibilities

  • Development of SAS programs and macros utilities pertaining to clinical trials: Tables of summary statistics and graphics for clinical aspects of clinical trials, Statistical PK analysis of bioequivalence trials.
  • Coordinate data transfers to and from external vendors.
  • Lead and Support multiple studies in generation of CDISC deliverables (SDTM, ADaM, and Define XML) and analysis outputs per regulatory guidance.
  • Other computer programs useful for the accomplishment of biometric department goals.
  • Analysis of existing processes and exploring improvement solutions.
  • Interacts with supervisor and other departments on process involving data and computer programs
  • Stay aware of regulatory guidelines and maintain computer programs and processes to be compliant.
  • Other related tasks

Desired profile

  • Masters/Bachelor degree in Statistics, Mathematics or Computer science
  • A minimum of 5 years of experience as SAS Programmer in the pharmaceutical and/or medical industry.
  • A minimum of 5 years of experience in data analysis is required.
  • Having experience in dealing with scientific affairs is a major asset.
  • Ability to interact with other staff members in order to understand and explain correctly and with accuracy the SAS programs, the data analyses and the application of software.
  • Ability to effectively handle multiple tasks and projects, under supervision.
  • Excellent accuracy and attention to detail.
  • Fluent in English speaking, reading and writing.
  • French is an asset
  • Software : SAS, different Microsoft softwares

Location:  Remote position can be based in either Canada or the US


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