Job Details

  • Title: SAS Programmer
  • Code: RCI-00004
  • Location: Mason, OH 45040
  • Posted Date: 11/24/2021
  • Duration: 17 Months
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  Job Description

Hours and Scheduling

  • 20 hour/week commitment – flexible but during standard business hours
  • Position opens the first week in February 2022
  • Onsite work is preferred (however, will not rule out offsite candidates)


PHCI Clinical Statistics Contractor - SAS Programmer

  • A SAS programmer is needed for a period of 1.5 years starting January 2022 to process and analyze clinical data arising from a clinical trial.
  • Candidates are expected to physically locate in and work from the Client Mason Business Center in Mason, OH.
  • Limited work from home options may be possible depending on business needs and COVID-19 pandemic developments.

 

Work Description

  • Write SAS code to review clinical data for errors, merge and otherwise prepare SAS datasets for efficacy and safety statistical analyses, create tabulated data summaries in RTF format with SAS Proc Report, and create figures with SAS SG procedures, suitable for direct incorporation into a final study report that conforms to ICH and eCTD standards/templates.
  • Prepare SAS datasets conforming to CDISC and ADaM standards for international regulatory agency submission.
  • All work will be done under the direction of a clinical statistician.
  • Job is not for writing applications, but for writing programs to analyze data
  • Must be proficient in programming in SAS for 1.5 yrs.
  • Individuals must have programmed at a pharmaceutical company or contract research organization writing SAS code for clinical research studies

 

Qualifications

  • B.S. or M.S. in Computer Science or another major of similar technical rigor
  • Proficiency programming in SAS
  • In depth experience working with clinical data conforming to CDISC and ADaM standards
  • Experience of producing tables listings and figures for direct incorporation into clinical study reports conforming to ICH and eCTD standards/templates
  • Average or better proficiency in Microsoft Office
  • Excellent problem-solving skills and attention to detail
  • Ability to work effectively with statisticians, analysts and project team members
  • Qualified candidates will have at least 3 years of experience processing clinical trial data with SAS
  • Proficiency with SAS programming is essential.
  • Write SAS code to review clinical data for errors, merge and otherwise prepare SAS datasets for efficacy and safety statistical analyses, create tabulated data summaries in RTF format with SAS Proc Report, and create figures with SAS SG procedures, suitable for direct incorporation into a final study report that conforms to ICH and eCTD standards/templates.
  • Prepare SAS datasets conforming to CDISC and ADaM standards for international regulatory agency submission.
  • All work will be done under the direction of a clinical statistician.

 

Work Experience

  • Qualified candidates will have at least 3 years of experience processing clinical trial data with SAS. Proficiency with SAS programming is essential.
  • Prepare SAS datasets conforming to CDISC and ADaM standards for international regulatory agency submission.
  • All work will be done under the direction of a clinical statistician.