Job Description
We are looking for motivated CRAs based in the Paris/Ile-de-France area to join our sponsor dedicated CRA team! Minimum 2+ years experience external monitoring of commercial studies with TA experience in oncology studies-phase I and III, involving a maximum of 2 or 3 protocols. As a Clinical Research Associate, you will be fully dedicated to one of our global pharmaceutical clients focused on oncology studies. This exclusive partnership offers a culture of innovation, flexibility, and collaboration to bring life-improving treatments to market. You'll have full ownership of investigator sites from study initiation to close-out, conduct feasibility, site selection, interim, and close-out visits, build strong relationships with investigator site staff to meet key clinical metrics, attend investigator meetings, and ensure proper shipment, storage, and accountability of clinical supplies, while monitoring data integrity and compliance with clinical trial guidelines.
About ICON plc
ICON plc is a world-leading healthcare intelligence and clinical research organisation that advances clinical research providing outsourced services.