Clinical Research Associate: On-Site Monitoring & Study Execution
Listed on 2026-10-15
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Research/Development
Clinical Research, Research Assistant/Associate, Research Scientist
IQVIA is seeking a Clinical Research Associate to perform monitoring visits, ensure data quality, and manage site communications in accordance with the study protocol and regulatory requirements.
The role requires at least 2 years of independent on-site CRA experience, a degree in a scientific field or health care, and solid knowledge of GCP/ICH guidelines. Strong problem-solving and organizational skills are essential.
We are seeking a motivated Clinical Research Associate:
On-Site Monitoring & Study Execution to join IQVIA in Oak Brook, IL, United States.
The following opportunity is for a Clinical Research Associate:
On-Site Monitoring & Study Execution with IQVIA.
Our group is growing, and we are hiring a Clinical Research Associate:
On-Site Monitoring & Study Execution in Oak Brook, IL, United States.
This opportunity is for the Clinical Research Associate:
On-Site Monitoring & Study Execution role at IQVIA.
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