Abstract: A method and system for identifying clinical trial sites is provided. The method includes receiving clinical trial data associated with a plurality of planned clinical trials. Portions of the clinical trial data are identified based on differing data sources. Relevant information is extracted from the portions. Socioeconomic data, demographics data, and epidemiological data are received and combined into a common format. Incorrect address data is corrected and the clinical trial data, socioeconomic data, demographics data, and epidemiological data are standardized. In response, an initial list is generated. The initial list includes associated principle investigators and clinical trial sites associated with planned clinical trials overlaid on the clinical trial data, the socioeconomic data, the demographics data, and the epidemiological data.

Abstract: A method and system for identifying clinical trial sites is provided. The method includes receiving clinical trial data associated with a plurality of planned clinical trials. Portions of the clinical trial data are identified based on differing data sources. Relevant information is extracted from the portions. Socioeconomic data, demographics data, and epidemiological data are received and combined into a common format. Incorrect address data is corrected and the clinical trial data, socioeconomic data, demographics data, and epidemiological data are standardized. In response, an initial list is generated. The initial list includes associated principle investigators and clinical trial sites associated with planned clinical trials overlaid on the clinical trial data, the socioeconomic data, the demographics data, and the epidemiological data.

Abstract: A method and system for identifying clinical trial sites is provided. The method includes receiving clinical trial data associated with a plurality of planned clinical trials. Portions of the clinical trial data are identified based on differing data sources. Relevant information is extracted from the portions. Socioeconomic data, demographics data, and epidemiological data are received and combined into a common format. Incorrect address data is corrected and the clinical trial data, socioeconomic data, demographics data, and epidemiological data are standardized. In response, an initial list is generated. The initial list includes associated principle investigators and clinical trial sites associated with planned clinical trials overlaid on the clinical trial data, the socioeconomic data, the demographics data, and the epidemiological data.

Abstract: A method and system for identifying clinical trial sites is provided. The method includes receiving clinical trial data associated with a plurality of planned clinical trials. Portions of the clinical trial data are identified based on differing data sources. Relevant information is extracted from the portions. Socioeconomic data, demographics data, and epidemiological data are received and combined into a common format. Incorrect address data is corrected and the clinical trial data, socioeconomic data, demographics data, and epidemiological data are standardized. In response, an initial list is generated. The initial list includes associated principle investigators and clinical trial sites associated with planned clinical trials overlaid on the clinical trial data, the socioeconomic data, the demographics data, and the epidemiological data.