Clinical Research Associate: Site Monitoring & Study Delivery
Listed on 2026-10-13
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Research/Development
Clinical Research, Research Assistant/Associate, Research Scientist -
Healthcare
Clinical Research
IQVIA is seeking a Clinical Research Associate to monitor and manage study sites, ensuring protocol adherence and regulatory compliance. You will perform site visits, support recruitment plans, and coordinate training with site staff.
The role requires 2+ years of on-site CRA experience, knowledge of GCP/ICH guidelines, and strong communication in English. Proficiency with EDC/CTMS/eTMF and MS Office is expected. IQVIA offers global opportunities and a collaborative environment.
Our team is growing, and we are hiring a Clinical Research Associate:
Site Monitoring & Study Delivery in Port Saint Lucie, FL, United States.
We invite applications for the Clinical Research Associate:
Site Monitoring & Study Delivery position located in Port Saint Lucie, FL, United States.
The following role is for a Clinical Research Associate:
Site Monitoring & Study Delivery with IQVIA.
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