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US-CT-Cheshire: Senior Clinical Programmer

Date: _02-Sep-2011_
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Senior Clinical Programmer I

· Independently create, execute, maintain, and validate programs that transfer data across multiple data management systems or operating systems. · Combine data from a variety of sources and structures, generate and store summary data from a variety of sources, generate reports or combine multiple relational databases. · Independently create, execute, maintain, and validate programs that generate edit checks, listings, tables and figures using SAS. Other Activities · Clearly document all work; manage assignments to meet timelines and produce high quality deliverables. · Perform other programming tasks as necessary to support Clinical Data Management. · Manage assignments to meet timelines and deliver high quality work as required. · Assume leadership responsibility as a contributing member of a multi-disciplinary clinical trials project team, communicating actively and frequently with other team members as needed. · Work efficiently and effectively with little direct supervision. Requirements · Masters degree in Computer Science or a related discipline, with 5-8 years of clinical programming experience or equivalent work experience that includes SAS/Base, SAS/Macro, SAS/SQL, SAS/Access in a windows environment.

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Developer FYI Center
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