Senior Clinical Research Associate – On-Site

Oxford Global Resources is seeking a Clinical Affairs support professional to help ensure study site selection and conduct in compliance with GCP and federal regulations. The role involves on-site monitoring activities and coordination of supplies across study sites, working with the Clinical Affairs team.The candidate should have 2+ years in clinical...

Overview In this role you support multicenter clinical studies by monitoring sites to ensure protocol adherence and data reporting per GCP/ICH guidelines. You will drive site communication, training, and recruitment alignment to project needs, and manage study progress and documentation in collaboration with the study team. The role includes ensuring TMF/ISF...

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

CRA / SENIOR CRA - Homebased (Italy)Temporary (1 year with possibility to be extended)TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and...

TFS HealthScience is seeking a Senior Clinical Research Associate to work remotely from Italy. You will monitor sites (on-site and remote), ensure data integrity and patient safety, and support regulatory compliance across studies in collaboration with project teams.The role requires 5+ years of trial monitoring experience, oncology exposure preferred, and...

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,...

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...

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...