Senior Clinical Research Associate: Site Monitoring & Trials
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Research/Development
Job Description & How to Apply Below
IQVIA Med Tech's MCRA unit seeks a Clinical Monitoring professional to perform site monitoring and site management to ensure studies are conducted per protocol, GCP/ICH guidelines, and sponsor requirements.
This on-site role in the Denver area partners with sites, manages recruitment, training, data quality, and TMF/ISF compliance, and collaborates with the study team to keep projects on track.
This role, Senior Clinical Research Associate:
Site Monitoring & Trials at IQVIA Inc, could be your next move.
The following opening is for a Senior Clinical Research Associate:
Site Monitoring & Trials with IQVIA Inc.
Our group is growing, and we are hiring a Senior Clinical Research Associate:
Site Monitoring & Trials in Denver, CO, United States.
This opening is for the Senior Clinical Research Associate:
Site Monitoring & Trials role at IQVIA Inc.
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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