Senior Oncology CRA - Lead Site Monitoring & Compliance
Listed on 2026-10-07
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Research/Development
Research Scientist, Clinical Research, Regulatory Compliance Specialist
IQVIA Biotech is seeking an experienced Senior Clinical Research Associate to join our Clinical Monitoring team. You will independently manage and monitor trial sites to ensure compliance with study protocols, GCP, ICH guidelines, FDA regulations, and sponsor expectations.
As a key study team member, you will perform site qualification, initiation, routine monitoring, and closeout visits. You will partner closely with investigative sites to support patient recruitment and retention efforts,
The Senior Oncology CRA
- Lead Site Monitoring & Compliance role at IQVIA Argentina is now open for applications in Overland Park, KS, United States.
We appreciate your interest in this position.
Join IQVIA Argentina 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 Senior Oncology CRA
- Lead Site Monitoring & Compliance role at IQVIA Argentina, based in Overland Park, KS, United States.
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