Faster ROI with rapidLIVE
"As we prepared to expand our services, we needed a reliable and feature-rich clinical data management system that the pharmaceutical industry knew and trusted. Oracle Clinical provides us with the functionality we need to help ensure quality services to pharmaceutical organizations through accurate clinical data capture and precise information management. PharmaSOL used the innovative "rapidLIVE" approach, which allowed for a quicker implementation of the full suite. The streamlined training and validation package simplified the system rollout and meant that users were immediately productive with the applications."
said Anna Jurczynska, Director of Business Development, Sermes CRO, 2010
Siebel Clinical
Oracle's Siebel Clinical Trial Management System offers a new and innovative approach to managing clinical trials. The approach focuses on strengthening relationships with trial participants, especially investigators and subjects, by using customer relationship management (CRM) software solutions.
Siebel Clinical Trial Management System enables global clinical organizations to maintain a centralized trial management database while providing a user with the most relevant and appropriate information based the their specific roles and responsibilities. Thus, real-time trial information is available not only to clinical research associates managing individual sites, but also to regional managers responsible for geographic areas as well as global trial managers managing global trials. Armed with the most current and relevant data, clinical users are able to spot problems earlier and take corrective actions sooner, thus reducing overall trial costs.
Using Siebel Clinical Trial Management System as a centralized repository for all investigators, clinical trial sponsors can collect and track all relevant information about their investigators, from personal profiles to disease specialties, from past trial experiences to current trial performance. By analyzing the comprehensive investigator data, clinical organizations are able to identify the investigators most suitable for a trial. Furthermore, Siebel Clinical Trial Management System can be used to provide personalized services to investigators by facilitating communications to the study team and by providing timely and accurate payments to investigators. The results are improved relationships with investigators, faster enrollment, better trial quality, and lower trial costs.
Siebel Clinical Trial Management System enables global clinical organizations to maintain a centralized trial management database while providing a user with the most relevant and appropriate information based the their specific roles and responsibilities. Thus, real-time trial information is available not only to clinical research associates managing individual sites, but also to regional managers responsible for geographic areas as well as global trial managers managing global trials. Armed with the most current and relevant data, clinical users are able to spot problems earlier and take corrective actions sooner, thus reducing overall trial costs.
Using Siebel Clinical Trial Management System as a centralized repository for all investigators, clinical trial sponsors can collect and track all relevant information about their investigators, from personal profiles to disease specialties, from past trial experiences to current trial performance. By analyzing the comprehensive investigator data, clinical organizations are able to identify the investigators most suitable for a trial. Furthermore, Siebel Clinical Trial Management System can be used to provide personalized services to investigators by facilitating communications to the study team and by providing timely and accurate payments to investigators. The results are improved relationships with investigators, faster enrollment, better trial quality, and lower trial costs.
