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Title:Sr. Statistical Programmer
Location:MA - Marlborough


Work as a statistical programmer on drug development project teams.

  • Support the inferential analysis of key safety and efficacy endpoints from clinical trials.
  • Primary responsibilities include the production of clinical trial deliverables (e.g. analysis datasets and specifications, well-documented SAS code, summary tables, figures, listings and analyses) for internal projects in support of internal biostatisticians, as well as providing validation and review of key results for external projects.
  • Programming of ad hoc requests for exploratory analyses and time-sensitive deliverables.
  • Develop global macro modules.
  • Provide team leadership within the programming function.

  • Bachelor or Masters level degree in Biostatistics, Statistics, or a related field.
    8+ years of pharmaceutical or biotech industry experience.
  • SAS experience is a requirement. Production of clinical study report deliverables, including analysis datasets, summary tables, figures and listings are relevant qualifications for this position.
  • Demonstrated, strong experience with SAS/GRAPH and SAS/STAT products is highly desired. Experience with SAS macros is essential.
  • Experience with regulatory submission, electronic submissions, and relational databases are desirable.
  • Must be able to work in a standardized programming environment and communicate results and work product both verbally and in writing.

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