Senior CRA: Global Trials

Trial Form Support seeks a capable Clinical Trial Monitor to oversee oncology trials across sites, ensuring patient safety, data integrity, and regulatory compliance from a home-based setting.Verifichi che le sue competenze e la sua esperienza corrispondano ai requisiti di questo ruolo, quindi si candidi con il suo CV qui sotto.You will coordinate monitoring...

Trial Form Support seeks a capable Clinical Trial Monitor to oversee oncology trials across sites, ensuring patient safety, data integrity, and regulatory compliance from a home-based setting. You will coordinate monitoring activities, manage documentation, and support audits to enable successful study execution.The role requires at least 3 years in...

ICON Plc is seeking a Senior Clinical Research Associate (CRA) to oversee clinical trial activities in Milan, Italy. You will monitor sites, ensure protocol adherence, and support trial execution while maintaining data integrity and participant safety.The role requires an advanced life sciences degree and extensive CRA experience, with travel up to 60% to...

Worldwide Clinical Trials S.r.I. is seeking a Clinical Research Associate (CRA) to join our Italy team. You will oversee site qualification, monitoring activities, and ensure data integrity across oncology and hematology studies, traveling as required.The ideal candidate has at least 2 years as a CRA, a 4-year degree (RN/BSN acceptable), and strong English...

Trial Form Support is seeking a remote Clinical Trial Monitor specializing in oncology to oversee site monitoring, data integrity, and regulatory compliance across global sites.Prima di candidarsi per questo ruolo, la preghiamo di leggere le seguenti informazioni su questa opportunità, riportate di seguito.You will ensure patient safety, validate informed...

Trial Form Support is seeking a remote Clinical Trial Monitor specializing in oncology to oversee site monitoring, data integrity, and regulatory compliance across global sites. You will ensure patient safety, validate informed consent, and manage trial documentation in line with GCP/ICH standards.In this home-based role, you will coordinate monitoring...

TFS HealthScience seeks a Clinical Research Associate (CRA) to join our team as a home-based professional in Italy.Qualifiche, competenze e l'esperienza necessaria per questo ruolo sono disponibili nella descrizione completa riportata di seguito.You will monitor sites, ensure subject safety and data integrity, and ensure compliance with GCP/ICH...

Fortrea is seeking a Senior Clinical Research Associate II to monitor and manage site activities for clinical trials in Italy.Se è interessato/a a candidarsi per questo lavoro, la preghiamo di assicurarsi di soddisfare i seguenti requisiti, elencati di seguito.You will lead monitoring efforts, ensure protocol and regulatory compliance, and support data...

TFS HealthScience seeks a Clinical Research Associate (CRA) to join our team as a home-based professional in Italy. You will monitor sites, ensure subject safety and data integrity, and ensure compliance with GCP/ICH guidelines.The role requires familiarity with regulatory processes and strong collaboration with project teams. The position offers a...