Clinical Research Associate - Site Monitoring & Impactful Trials
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Research/Development
Job Description & How to Apply Below
IQVIA is seeking an on-site Clinical Research Associate to monitor study sites, ensure protocol compliance, and manage data and regulatory submissions. You will train sites, track recruitment, and maintain TMF/ISF documentation while collaborating with the study team.
Required qualifications include 2+ years of CRA experience, strong GCP/ICH knowledge, and proficiency with EDC/CTMS systems. Fluency in English and excellent communication skills are essential.
As a Clinical Research Associate
- Site Monitoring & Impactful Trials, you will play an important part at IQVIA in Barre, VT, United States.
The following role is for a Clinical Research Associate
- Site Monitoring & Impactful Trials with IQVIA.
Our organisation is growing, and we are hiring a Clinical Research Associate
- Site Monitoring & Impactful Trials in Barre, VT, United States.
This role is for the Clinical Research Associate
- Site Monitoring & Impactful Trials 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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