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Clinical SAS Programmer
South San Francisco, CA, US
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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