Clinical Research Associate: Site Monitoring & Execution
Listed on 2026-10-15
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Research/Development
Clinical Research, Research Assistant/Associate
IQVIA is seeking a Clinical Research Associate (CRA) to monitor study sites in accordance with the protocol, GCP, and sponsor requirements. You will perform site visits, manage recruitment tracking, and ensure data quality and regulatory compliance across assigned studies.
The role requires on-site monitoring experience, strong communication, and proficiency with EDC/CTMS/eTMF systems, along with English-language proficiency.
We are seeking a motivated Clinical Research Associate:
Site Monitoring & Execution to join IQVIA in New York, NY, United States.
The position is based in New York, NY, United States.
This opportunity is part of our work in Bio & Pharmacology & Health.
The advertised compensation is 75..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Clinical Research Associate:
Site Monitoring & Execution role in the description above.
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