SAS Programmer III

Location: South San Francisco, California
Posted On: 7/6/2017
Job Code: 4857_SAS_CA
Job Description
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. Write, test and validate SAS programs to produce analysis datasets, TLGs and presentation output, to be included in reports for submission to regulatory agencies, publications and other communications.
Write CDSIC standard dataset specifications and follow specifications to create SDTM and ADaM datasets. Understand and execute department-, product- and study-level macros and utilities. Write, test and validate product- and study-level macros and utilities. 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.

Additional Skills:
Strong SAS Programming skills Extensive hands-on experience in CDSIC standards and datasets (SDTM, ADaM) Experience in FDA/EMEA trial submissions Drug Development (pre-, early, late and/or observational) in related industries or academic research
Category:IT  code:new
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Contact Details
Ajay Rajauriya