Senior Clinical Research Associate

If you are an experienced Senior CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you!Scorra verso il basso per trovare i dettagli completi dell'offerta, inclusa l'esperienza richiesta e le mansioni associate.Translational Research in Oncology (TRIO)is a global clinical research...

OverviewSe è interessato/a a candidarsi per questo lavoro, la preghiamo di assicurarsi di soddisfare i seguenti requisiti, elencati di seguito.In this home-based role, you will monitor clinical trials in oncology across sites, ensuring patient safety, data integrity, and regulatory compliance. You'll work within the Strategic Resourcing Solutions team to...

Overview In this home-based role, you will monitor clinical trials in oncology across sites, ensuring patient safety, data integrity, and regulatory compliance. You’ll work within the Strategic Resourcing Solutions team to support study conduct, site management, and quality by adhering to GCP/ICH and SOPs. You’ll coordinate monitoring activities, manage...

If you are an experienced Senior CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you!Le interessa questa opportunità? Si candidi in fretta, è previsto un elevato volume di candidature. Scorra verso il basso per leggere la descrizione completa.Translational Research in Oncology...

Trial Form Support is seeking a remote Monitoring Specialist to oversee oncology clinical trials across sites, ensuring patient safety, data integrity, and regulatory compliance per GCP/ICH and SOPs.Possiede le competenze per ricoprire questo ruolo? Legga i dettagli completi qui sotto e invii la sua candidatura oggi stesso.Based in a globally collaborative...

Trial Form Support is seeking a remote oncology clinical monitors to oversee trials across sites, ensuring patient safety, data integrity and regulatory compliance in a fast-paced setting.The role supports study conduct, site management and quality with GCP/ICH adherence, coordinating monitoring activities and audits while enabling meaningful patient...

Provide support to Clinical Affairs team to assure study site selection and conduct of the study by study sites in compliance with Good Clinical Practices, federal regulations, and Clinical Affairs SOPs through in-house and some on-site monitoringConduct pre-study visits to assure the site has adequate facilities, staff, and subject population for conducting...

Clinical Research Associate II / Senior Clinical Research (CRA) - Italy Job Category : Clinical MonitoringRequisition Number : CLINI002065Posted : October 1, 2026Full-TimeRemoteLocations Showing 1 locationItaly - RemoteDescriptionWhatYou'llDo:Serve as main CTI contact for assigned study sitesConduct site visits (pre-study [PSV], site initiation [SIV],...

Overview In this role, you will lead site management and monitoring for assigned trials to ensure patient safety and high-quality execution. You will work with cross-functional teams to keep study activities on track from activation to database lock. You will monitor AEs/SAEs and support Drug Safety, audits, and CAPA implementation. This is a remote,...