Clinical Research Monitor II - Site & Data Integrity
Listed on 2026-10-11
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Research/Development
Clinical Research, Research Assistant/Associate -
Healthcare
Clinical Research
IQVIA Med Tech seeks a Clinical Monitoring Specialist to perform site monitoring and site management, ensuring studies are conducted per protocol, GCP and ICH guidelines. You will communicate with sites, track recruitment and data query resolutions, and support TMF/ISF filing.
You will collaborate with the study team to ensure quality data and regulatory compliance across trials in medical device and diagnostics sectors.
Join us at iqvia as our next Clinical Research Monitor II
- Site & Data Integrity in Washington, DC, United States.
Our organisation is growing, and we are hiring a Clinical Research Monitor II
- Site & Data Integrity in Washington, DC, United States.
This opportunity is for the Clinical Research Monitor II
- Site & Data Integrity role at iqvia.
We are seeking a motivated Clinical Research Monitor II
- Site & Data Integrity to join iqvia in Washington, DC, United States.
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