IQVIA is seeking a Clinical Research Associate to perform site monitoring visits and ensure studies are conducted per protocol and regulations.
Di seguito, troverà un'analisi completa di tutti i requisiti per i potenziali candidati e le istruzioni su come candidarsi. In bocca al lupo!
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. xkiyazw
Strong English and MS Office skills are expected; some site financial tasks may be required.
📌 Clinical Research Associate: Site Monitoring & Study Delivery (Milano)
🏢 Iqvia
📍 Milano