Clinical Research Associate: Site Monitoring Pro
Listed on 2026-10-18
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Research/Development
Clinical Research, Research Assistant/Associate, Research Scientist
IQVIA in the United States is seeking a Clinical Research Associate with on-site monitoring experience to ensure sites conduct studies per protocol, GCP, and regulatory requirements. The role involves coordinating recruitment plans, training sites, and tracking data integrity.
The candidate will manage site submissions, CRF completion, and data queries, while maintaining essential study documentation and fostering cross-functional collaboration with the study team.
This role, Clinical Research Associate:
Site Monitoring Pro at IQVIA, could be your next career step.
The position is based in Abilene, TX, 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 Pro role in the description above.
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