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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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Thank you,
Developer FYI Center
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