Katalyst CRO

Clinical SAS Programmer

South San Francisco, CA, US

23 days ago
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Summary

Responsibilities

  • Performs all SAS programming required for clinical trial analysis and reporting.
  • Ensures that activities and processes performed are conducted according to sponsor requirements.
  • Works closely with the Biostatistics and Data Management departments on various clinical projects.
  • Designs and/or reviews database structure.
  • Writes edit checks from the Data Cleaning Plan (DCP) specifications.
  • Creates derived-analysis datasets.
  • Executes analyses specified in the Statistical Analysis Plan (SAP) or Report and Analysis Plans (RAP) under the guidance of the project statistician.
  • Acts as primary programmer to produce tables, listings, and figures for the clinical study report (CSR).
  • Acts as secondary programmer to validate SAS programs that produce derived-analysis datasets and data analyses.

Requirements:

  • Leads programming efforts for large complex studies.
  • Requires time management skills, and strong SAS programming expertise.
  • Reviews case report form (CRF) design.
  • Years of Experience 5-7.

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