SAS Clinical Statistician

Chivalry Consulting, Inc. - North Chicago, IL

Contract

This is an onsite W2 contract-to-hire position. We are unable to do corp-to-corp, or sponsor H1B Visas at this time.

SAS Clinical Statistician

Responsibilities

  • Provide statistical expertise for study case report for design, data base structure, analysis plan, and review of the study protocols and reports.
  • Perform data analysis and provide statistical support including collaboration with medical groups to complete joint scientific reports and FDA overviews, including review of such reports to ensure accuracy and clarity.
  • Review analysis output to ensure internal consistency with other output for various reports such CSR, ISS, ISE.
  • Responsible for the accuracy of SAS programs by reviewing output, reviewing code, reviewing log files and running all checking utilities.
  • Responsible for creating peer review programs for assigned studies.
  • Ensure all SAS programs are imported into the archive system prior to the creation of final output.
  • Responsible for the creation and accuracy of derivation programs for routine and complicated analyses, including peer review.
  • Responsible for the creation and accuracy of all submission data sets and analysis programs.
  • Responsible for the creation of data definition documents and TOCs.
  • Learn and maintain expertise in the use of the UNIX utilities developed for the Statistical Programmers. Participate in the development of new UNIX utilities and SAS macros.
  • Provide accurate and timely responses to routine requests from clients.

Qualifications

  • Must have clinical research experience.
  • Demonstrated thorough understanding of SAS programming concepts and techniques.
  • CDISC (ADaM and SDTM) experience.
  • Communication and time management.
  • Unix experience.
  • 8+ year plus MS in Statistics or Computer, or 10+ years plus Bachelor’s in Statistics or Computer.
  • Experience working on regulatory submissions.

Job Type: Contract

Salary: $60.00 /hour

Experience:

  • Clinical Trial: 1 year (Required)
  • CDISC (ADaM and SDTM): 1 year (Required)
  • UNIX: 2 years (Required)
  • Regulatory Submissions: 1 year (Preferred)
  • SAS Programming: 3 years (Required)

Education:

  • Bachelor's (Required)