Clinical Research Technology S.r.l
Clinical Research Technology S.r.l. (CRT) is a Contract Research Organization that was established in 1999. It specializes in the management of clinical trials, ensuring adherence to Good Clinical Practice (ICH/GCP) standards. CRT's scope of work includes the handling of Phase I-IV clinical trials, as well as observational studies, medical device studies, epidemiological studies, and pharmacoeconomic studies. A key aspect of CRT's operations involves the development and implementation of web-based platforms for clinical data management, utilizing innovative technologies to enhance trial efficiency and data quality. The organization provides a comprehensive range of services across various therapeutic areas, including oncology, cardiology, and infectious diseases. Additionally, CRT offers support in regulatory affairs, data management, statistical analysis, and pharmacovigilance. A strong emphasis is placed on the use of technological innovation to improve clinical trial outcomes while reducing both time and costs. In essence, CRT supports other companies in conducting clinical trials by leveraging modern technology.
Role
Clinical Research Technology S.r.l. (CRT) will manage the local project management, site selection, regulatory affairs, and site monitoring activities for the Italian centers within the GIM network participating in the Path-for-young project.
Members
Paola Schiavo
Project Manager with extensive expertise in oncology clinical trial management, guaranteeing efficient oversight and strategic direction.
Vittoria Palmieri
Clinical Trial Administrator - will manage administrative tasks, documentation, and communication, facilitating smooth project operations.
Eleonora Rizzuti
Clinical Research Associate (CRA) - will be responsible for on-site monitoring and data verification, ensuring adherence to protocol and quality standards.
Francesca Cerrone
Clinical Trial Administrator - will manage administrative tasks, documentation, and communication, facilitating smooth project operations.
Danilo Spadavecchia
Regulatory Specialist - will handle all task related to regulatory submissions and manage regulatory compliance throughout the study, ensuring adherence to all applicable guidelines and requirements.
Pasqualina Di Caprio
Clinical Trial Administrator - will manage administrative tasks, documentation, and communication, facilitating smooth project operations.
Annarita D'Andrea
Rita Pepe
Clinical Research Associate (CRA), will be responsible for on-site monitoring and data verification, ensuring adherence to protocol and quality standards