Clinical Research Associate: Site Monitoring

15 ott - Milano
Iqvia

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 MS Office skills are expected; some site financial tasks may be required.
J-18808-Ljbffr

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