Clinical Research Associate: Site Monitoring

OverviewSebbene l'esperienza professionale e le qualifiche siano fondamentali per questo ruolo, si assicuri di verificare di possedere le soft skill preferenziali, se richieste, prima di candidarsi.In this home-based role, you will monitor clinical trials in oncology across sites, ensuring patient safety, data integrity, and regulatory compliance. You'll...

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],...

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!Translational Research in Oncology (TRIO)is a global clinical research organizationdedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is...

Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a...

CTI is seeking a Clinical Research Associate II / Senior CRA to support sites in Italy, focusing on regulatory compliance and timely deliverables. You will act as the main CTI contact for assigned sites and manage site visits throughout pre-study through close-out phases.The role requires 3–5 years of CRA experience with a strong life-science background,...

Syneos Health, Inc. is seeking a CRA II Italia - Home Based to support site qualification, initiation, monitoring and close-out visits. You will ensure regulatory compliance, verify informed consent, and protect patient data integrity across trial sites.The role requires excellent communication, presentation and interpersonal skills, with up to 75% travel. A...

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 Clinical Monitor to oversee oncology trials across sites, ensuring patient safety, data integrity, and regulatory compliance. You will coordinate monitoring activities, manage documentation, and participate in audits while supporting study conduct within a global, collaborative team.The role requires a Bachelor's in...

Overview As Clinical Research Manager (CRM) in Ophthalmology, you lead clinical operations across multiple studies and countries. You will ensure compliance with ICH-GCP, SOPs, and contracts while partnering with PMs, CRAs, sponsors, and sites. This role focuses on delivering trials on time, in scope, and to high quality, within a global CRO environment....