Senior Clinical Research Associate – On-Site

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...

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...

Senior Clinical Research Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and...

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. Potrebbe essere proprio lei il candidato/la candidata ideale per questo lavoro. Legga tutte le informazioni associate e invii la sua candidatura.As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability,...

SENIOR CRA - HOMEBASED ITALYTFS 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 Functional Service (FSP) solutions.Join Our Team as a Senior...

Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with...

Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.Essential FunctionsPerform site monitoring visits (selection, initiation, monitoring and close‑out visits) in accordance with...

Clinical Research Associate II / Senior Clinical Research (CRA) - Italy Job Category : Clinical Monitoring Requisition Number : CLINI Posted : October 1, 2026 Full-Time Remote Locations Showing 1 location Italy - RemoteDescription WhatYou'llDo: Serve as main CTI contact for assigned study sites Conduct site visits (pre-study (PSV), site initiation (SIV),...

IQVIA is seeking a Clinical Research Associate to perform site monitoring visits and ensure studies are conducted per protocol and regulations. You will manage site communications, training, and documentation.You will track recruitment, CRF completion, data queries, and regulatory submissions, and support start-up and TMF/ISF maintenance. Strong English and...