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Responsible for building programs to create SAS datasets from the clinical database, external data sources, and other sources while following the clinical study’s protocol or statistical plans.


  • Develop programs for data transfers and assist in their review to ensure the data transfer has been produced to specification.
  • Develop good problem-solving skills and a willingness to learn and seek advice from senior Statistical Programming staff.
  • Carry out all activities according to Covance SOPs working within the framework of the Quality Management System and to Good Clinical Practice (GCP).
  • Perform other duties as assigned by senior Programming staff.
  • Become familiar with clinical trial data and drug development process.
  • Develop SAS programs and output to create ADaM and client-defined analysis datasets, tables, listings and graphs.


  • Strong communication, interpersonal, organization, leadership and critical thinking skills
  • Ability to work in a team environment
  • Entry-level candidate may also apply

How to apply

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