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SAS Programmers United States, Cambridge United States,  

Navitas Life Sciences (company)

Posted on : 22 December 2017

Project Description

Category: Experienced (non-manager)
Location: New Jersey and Cambridge MA
Job Type:
Full Time
Education: Graduate Degree

Job Description:

  • Candidates will be expected to do both production and QC programming of SDTM datasets, analysis datasets, tables, listings, and figures, for multiple clinical trials using SAS software.
  • Must be able to work with minimal supervision under the direction of a lead programmer.
  • Must be able to effectively and timely communicate issues to lead programmer or manager.
  • Must meet timelines or communicate proactively and effectively if timelines are at risk so that mitegating plans can be adjusted and/or executed.

Preferred Skills:

  • Must be highly knowledgeable in the field of statistical programming.
  • Must be able to recognize when negotiating skills are needed and seek assistance when necessary.
  • Excellent organizational, interpersonal, and communication skills are a must; essential function of the role.
  • 5 + years SAS programming including SAS STAT, GRAPH and MACRO
  • 5 + years relevant industry experience
  • Extensive knowledge of drug development process and clinical trials
  • Extensive knowledge of drug submission requirements, relevant ICH and FDA/EMEA guidelines, CDISC standards

If you would like to apply for this position, or would like a discussion about this, or any other role, please send your contact details, together with your curriculum vitae to:


New JerseyCambridge MA North America

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