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US-MA-Waltham: Sr. SAS Programmer

Date: _29-Oct-2013_
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Sr. SAS Programmer

Design, develop, evaluate, validate and modify computer programs using SAS to analyze and evaluate clinical data Produce and deliver standard datasets, program edit checks and produce quality tables, figures and listings in a timely fashion and high quality Posess thorough knowledge of CDISC theory and implementation guidelines, able to create and validate CDISC standard datasets Provide expertise in the design and development of clinical trials, protocols, case report forms and clinical databases Work closely with clinical operations, data management and statisticians on various clinical projects so that data analysis can be performed in a timely fashion Liaise with vendors as needed to facilitate electronic data transfers

Good written and oral presentation skills and ability to communicate effectively to other programmers and non-technical colleagues Ability to think creatively and independently, and to form sound opinions and make sensible decisions in a dynamic environment Extensive experience working with data management on data checking to ensure locked database in pristine quality Minimum Bachelor's degree or equivalent level of experience

Experience 5+ years in a pharmaceutical/biotech, CRO setting R programming experience, a plus

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