{"id":1804,"date":"2025-06-26T11:50:02","date_gmt":"2025-06-26T09:50:02","guid":{"rendered":"https:\/\/path-for-young.unicancer.fr\/?post_type=partner&#038;p=1804"},"modified":"2025-08-01T16:29:17","modified_gmt":"2025-08-01T14:29:17","slug":"clinical-research-technology-s-r-l","status":"publish","type":"partner","link":"https:\/\/path-for-young.unicancer.fr\/es\/partner\/clinical-research-technology-s-r-l\/","title":{"rendered":"Clinical Research Technology S.r.l."},"content":{"rendered":"\n<div class=\"wp-block-uagb-container uagb-block-ef18c2f7 alignwide uagb-is-root-container\">\n<div class=\"wp-block-uagb-container uagb-block-7413f8a5\"><div class=\"plmb plmb-text mce-content clearfix format-classic resp-format-mob-title-center\">\r\n\t<h2>Clinical Research Technology S.r.l<\/h2>\n<p>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.<\/p>\n<\/div>\r\n<\/div>\n\n\n\n<div class=\"wp-block-uagb-container uagb-block-0aa2c650\"><div class=\"plmb plmb-text mce-content clearfix format-classic\">\r\n\t<h2><span style=\"color: #006160\">Role<\/span><\/h2>\n<p>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.<\/p>\n<\/div>\r\n<\/div>\n<\/div>\n\n\n\n<div class=\"wp-block-uagb-container uagb-block-b2467a3b alignwide uagb-is-root-container\"><div class=\"plmb plmb-text mce-content clearfix format-classic resp-format-mob-title-center\">\r\n\t<h2>Members<\/h2>\n<\/div>\r\n<\/div>\n\n\n\n<div class=\"wp-block-uagb-container uagb-layout-grid uagb-block-bdd08094 alignwide uagb-is-root-container\">\n<div class=\"wp-block-uagb-container partners-member-item uagb-block-29a236fe\"><div class=\"plmb plmb-text mce-content clearfix format-classic\">\r\n\t<h3>Paola Schiavo<\/h3>\n<p>Project Manager with extensive expertise in oncology clinical trial management, guaranteeing efficient oversight and strategic direction.<\/p>\n<\/div>\r\n<\/div>\n\n\n\n<div class=\"wp-block-uagb-container partners-member-item uagb-block-d0a79992\"><div class=\"plmb plmb-text mce-content clearfix format-classic\">\r\n\t<h3>Vittoria Palmieri<\/h3>\n<p>Clinical Trial Administrator  - will manage administrative tasks, documentation, and communication, facilitating smooth project operations.<\/p>\n<\/div>\r\n<\/div>\n\n\n\n<div class=\"wp-block-uagb-container partners-member-item uagb-block-0eeb73c3\"><div class=\"plmb plmb-text mce-content clearfix format-classic\">\r\n\t<h3>Eleonora Rizzuti<\/h3>\n<p>Clinical Research Associate (CRA) - will be responsible for on-site monitoring and data verification, ensuring adherence to protocol and quality standards.<\/p>\n<\/div>\r\n<\/div>\n\n\n\n<div class=\"wp-block-uagb-container partners-member-item uagb-block-f22493d1\"><div class=\"plmb plmb-text mce-content clearfix format-classic\">\r\n\t<h3>Francesca Cerrone<\/h3>\n<p>Clinical Trial Administrator  - will manage administrative tasks, documentation, and communication, facilitating smooth project operations.<\/p>\n<\/div>\r\n<\/div>\n\n\n\n<div class=\"wp-block-uagb-container partners-member-item uagb-block-429aff09\"><div class=\"plmb plmb-text mce-content clearfix format-classic\">\r\n\t<h3>Danilo Spadavecchia<\/h3>\n<p>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.<\/p>\n<\/div>\r\n<\/div>\n\n\n\n<div class=\"wp-block-uagb-container partners-member-item uagb-block-d0f60b58\"><div class=\"plmb plmb-text mce-content clearfix format-classic\">\r\n\t<h3>Pasqualina Di Caprio<\/h3>\n<p>Clinical Trial Administrator  - will manage administrative tasks, documentation, and communication, facilitating smooth project operations.<\/p>\n<\/div>\r\n<\/div>\n\n\n\n<div class=\"wp-block-uagb-container partners-member-item uagb-block-cd252deb\"><div class=\"plmb plmb-text mce-content clearfix format-classic\">\r\n\t<h3>Annarita D'Andrea<\/h3>\n<\/div>\r\n<\/div>\n\n\n\n<div class=\"wp-block-uagb-container partners-member-item uagb-block-20103733\"><div class=\"plmb plmb-text mce-content clearfix format-classic\">\r\n\t<h3>Rita Pepe<\/h3>\n<p>Clinical Research Associate (CRA),  will be responsible for on-site monitoring and data verification, ensuring adherence to protocol and quality standards<\/p>\n<\/div>\r\n<\/div>\n<\/div>\n","protected":false},"featured_media":1696,"template":"","class_list":["post-1804","partner","type-partner","status-publish","has-post-thumbnail","hentry"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.8 - 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