Clinical Research Associate - Site Monitoring & Study Execution
Listed on 2026-10-15
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Research/Development
Research Assistant/Associate, Clinical Research, Research Scientist, Biotech Research
IQVIA is seeking a Clinical Research Associate to monitor trial sites and ensure data integrity in line with the study protocol and ICH/GCP guidelines. The role involves initiating and close-out visits, site training, and ongoing communication with investigators to manage expectations and issues.
You will track regulatory submissions, patient recruitment, and data queries, while ensuring Study Files are complete and compliant.
As a Clinical Research Associate
- Site Monitoring & Study Execution, you will play an important part at IQVIA in Kansas City, MO, United States.
This role, Clinical Research Associate
- Site Monitoring & Study Execution at IQVIA, could be your next move.
Are you ready to take on the Clinical Research Associate
- Site Monitoring & Study Execution role at IQVIA?
We would love to welcome a new Clinical Research Associate
- Site Monitoring & Study Execution to our group in Kansas City, MO, United States.
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