Senior Oncology CRA - Lead Site Monitoring & Compliance

IQVIA · Overland park, United States

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,