Clinical Research Associate: Site Monitoring

Overview In this CRA role at Medpace you will support the integrity of clinical studies across pharmaceutical and medical device development. You’ll join a training-focused program (PACE) that accelerates your skills toward independent CRA responsibilities. You work across sites, regulators, and cross-functional teams to ensure compliant trials and data...

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...

Overview As a CRA II at ICON, you contribute to designing and analyzing clinical trials, ensuring data quality and patient safety while supporting investigators and site staff. You’ll work cross-functionally to monitor trials, resolve data queries, and prepare key study documents. This role sits at the heart of advancing new medicines, offering...

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...

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...

Overview In this role you join Medpace's Clinical Monitoring team in Italy to perform site monitoring, qualification, initiation, and closeout visits while ensuring protocol and regulatory compliance. You will verify investigator qualifications, manage data integrity, and support site performance to drive successful clinical trials. Travel up to 60-80%...

Overview In this role you will oversee clinical trial activities to ensure protocol alignment, regulatory compliance, and data integrity. You will monitor sites, conduct visits, and collaborate with cross-functional teams to support timely data collection and trial execution. You will train site staff, build strong relationships, and drive high standards of...

Overview In this role you oversee clinical trial monitoring to ensure adherence to protocol, regulatory standards and GCP, driving quality and continuous improvement. You will lead site visits, collaborate with cross-functional teams and mentor site staff, ensuring smooth trial execution. Your work supports ICON’s mission to bring new medicines to patients...