- ICON Clinical Research (MN)
- …sources (eg, Lab data, Site data). + Batch import agreed data sources into the EDC system. + Develop, program, validate, and maintain Medidata Rave EDC clinical ... trial databases in accordance with company standards. + Create EDC design specifications encompassing the data dictionary, event definitions, electronic consent,… more
- Lilly (Indianapolis, IN)
- …life better for people around the world. The Clinical Study Build Programmer is responsible for programming and testing clinical trial data collection databases, ... 11 etc. + Knowledge of industry standard clinical technologies including CTMS, EDC (Veeva CDMS preferred, Rave, InForm), eCOA, IxRS, Clinical Data Repositories, etc.… more
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