Clinical Research Associate II — On-Site Monitoring Pro
Listed on 2026-10-20
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Research/Development
Research Assistant/Associate, Clinical Research
IQVIA is seeking a Clinical Research Associate II with independent on-site monitoring experience to join our team in the United States. You will conduct site selection, initiation, routine monitoring, and closeout visits in accordance with GCP, ICH, and applicable regulatory requirements while training site staff.
You will build strong investigator relationships, monitor progress, ensure TMF readiness, prepare monitoring reports, and collaborate with cross-functional teams to support patient
Are you ready to take on the Clinical Research Associate II — On-Site Monitoring Pro role at IQVIA?
The following role is for a Clinical Research Associate II — On-Site Monitoring Pro with IQVIA.
Our organisation is growing, and we are hiring a Clinical Research Associate II — On-Site Monitoring Pro in Durham, NC, United States.
This role is for the Clinical Research Associate II — On-Site Monitoring Pro role at IQVIA.
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