Clinical Research Associate: Site Monitoring & Study Delivery
Listed on 2026-10-16
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Research/Development
Clinical Research, Research Assistant/Associate
IQVIA is seeking a Clinical Research Associate to monitor study sites and ensure data quality according to protocol and regulations. You will manage site communications, training, and documentation, and coordinate with the project team to maintain timelines and deliverables.
Responsibilities include coordinating recruitment, handling regulatory submissions, and ensuring TMF/ISF readiness. Strong English skills and experience with GCP/ICH are required, along with proficiency in common trial
Our group is growing, and we are hiring a Clinical Research Associate:
Site Monitoring & Study Delivery in Cheyenne, WY, United States.
The position is based in Cheyenne, WY, 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.
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