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Performs all SAS programming required for clinical trial analysis and reporting. Ensures activities and processes align with sponsor requirements. Collaborates closely with the Biostatistics and Data Management departments on various clinical projects. Leads programming efforts for large, complex studies. Demonstrates strong time management skills and SAS programming expertise. Reviews case report form (CRF) design. Designs and reviews database structures. Writes edit checks from Data Cleaning Plan (DCP) specifications. Creates derived-analysis datasets. Executes analyses as specified in the Statistical Analysis Plan (SAP) or Report and Analysis Plans (RAP) under the guidance of the project statistician. Acts as the 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. Required experience: 5-7 years.
#J-18808-Ljbffr...HR Manager Athens, AL (Job Code: S01760) Location: Athens, Alabama (On-Site) Employment Type: Full-Time | Exempt Department: Human Resources Reports To: Director Global Corporate Human Resources Supervises: HR Specialists and HR Support Staff About...
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