Clinical Research Associate: Site Monitoring & Study Oversight
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Research/Development
Job Description & How to Apply Below
IQVIA is seeking an experienced Clinical Research Associate to monitor study sites and ensure data integrity in line with the protocol, regulations, and sponsor requirements. The role requires engaging with sites to drive recruitment plans, administer protocol training, and maintain clear communications throughout the study lifecycle.
The ideal candidate has 2+ years of on-site CRA experience, strong knowledge of GCP/ICH guidelines, and proficiency with EDC, CTMS, and eTMF systems, alongside
Step into the Clinical Research Associate:
Site Monitoring & Study Oversight role at IQVIA Inc in Springfield, OH, United States and grow with us.
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.
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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