Clinical Research Associate: Site Monitoring & Study Delivery
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Research/Development
Job Description & How to Apply Below
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
We are currently recruiting a Clinical Research Associate:
Site Monitoring & Study Delivery for our team in Cheyenne, WY, United States.
The following opening is for a Clinical Research Associate:
Site Monitoring & Study Delivery with IQVIA.
Our team is growing, and we are hiring a Clinical Research Associate:
Site Monitoring & Study Delivery in Cheyenne, WY, United States.
This opening is for the Clinical Research Associate:
Site Monitoring & Study Delivery role at IQVIA.
Position Requirements
10+ Years work experience(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
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