•Create and execute SAS programs for datasets, tables, listings, and figures in support of clinical study reports and other clinical deliverables.
•Provide overall quality review of all SAS output within agreed-upon project timelines, in conjunction with other Aeras SAS Programmers and the project statistician.
•Document and effectively manage all relevant documentation per SOPs and GCP standards for designs, scripts, and other processes.
•5 years minimum SAS programming experience, including use of base SAS, SAS/STAT, and SAS macro language, in a biotech or pharmaceutical company, or contract research organization servicing the pharmaceutical industry.
•Familiarity with the regulatory environment for production of table and listings, including familiarity with GCP standards and good documentation practice.
•Familiarity with Clinical Data Interchange Standards Consortium (CDISC) standards for programming of derived datasets.
•Experience using the SAS Output Delivery System to output tables and listings.
•Experience developing SAS macros systems a plus.
•Experience with extracts to SAS from Electronic Data Capture (EDC) systems used for clinical trials research.
•Proven ability to be innovative, set realistic timelines, and provide programming insight and leadership as part of a clinical study project team.
•Excellent communication skills and ability to function as a lead team member on clinical trial project teams.
•BA or BS degree in Computer Science, Statistics, or related field
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