SAS Programming

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. It is preferred that the candidate is familiar with Unix platform and/or CDISC standards. Candidate MUST be able to complete a 1 year assignment. No OT, No Travel required. All work to be performed onsite in Madison.

Graduated

Kashish Vermani

IT Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I

Direct: 732-429-1912 (W) 732-549-2030 x 232 | (F) 732-549-5549

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