Clinical SAS Programmer

Title: SAS Programmer III

Location: San Francisco, CA

Duration: 18 Months

Job Description

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

Regards,

Anuj Mehta

703-889-6624