Las Vegas , NV , United States
Develop data file structure and layout specifications for transfer of study related external electronic data for loading into database. This will include CRF/eCRF specifications design data collection screen design database setup edit check programming defining external data transfer specifications database setup for external data and batch loading of external data on an ongoing basis.
• Create CRF/eCRF specifications with data management ensuring consistency with the protocol. • Design and implement databases to facilitate efficient data capture. • Create EDC and paper CRF annotations defining the data collection structure. • Review the study-specific edit check specifications and program the corresponding edit checks. • Support all Database Design activities for Clinical Systems. • Responsible for the set up of the database and the loading of the data into the database for the study related external electronic data received.
Requirements: • A minimum of six (6) years experience as a database developer and edit check programmer in the pharmaceutical/biotechnology industry is required. • A minimum of 3 years experience with Clintrial or similar clinical data management system or web-based EDC data collection application. • Working knowledge of Oracle SQL PL/SQL and SQL Loader. • Knowledge of Visual Basic and HTML/XML programming. • Experience in dealing with external sources of data (i.e. CROs central labs). • Strong written and oral communications skills and effective listening skills. • Working knowledge of database structures and design clinical study development and data collection workflow processes. • Experience in designing CRFs for clinical studies is a plus.
• EDUCATION: B.S.
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