CRA, Early Development — On-Site Monitoring
Listed on 2026-10-20
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Research/Development
Research Scientist, Clinical Research, Research Assistant/Associate
IQVIA in the United States is seeking a dedicated Clinical Research Associate (CRA) to monitor and manage clinical sites, ensuring protocol adherence, regulatory compliance, and sponsor expectations. Your work will contribute to data integrity.
You will conduct site visits (selection, initiation, monitoring, close-out) per GCP/ICH guidelines, support subject recruitment, provide protocol training, and collaborate with cross-functional teams to ensure study goals are met.
The following opportunity is for a CRA, Early Development — On-Site Monitoring with IQVIA.
Learn more about the CRA, Early Development — On-Site Monitoring role in the description above.
We appreciate your interest in this position.
Join IQVIA and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the CRA, Early Development — On-Site Monitoring role at IQVIA, based in Carlsbad, CA, United States.
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