Clinical Research Associate: On-Site Monitoring & Coordination

IQVIA is seeking a Clinical Research Associate to monitor study sites, ensure data integrity, and drive subject recruitment plans in line with the protocol and regulatory standards. The role requires on-site visits, strong communication with sites, and collaboration with the study team to manage expectations and issues.

You will ensure TMF/ISF readiness, track regulatory submissions, and support start-up activities where needed.

The Clinical Research Associate:
On-Site Monitoring & Coordination position in the Bio & Pharmacology & Health, Management & Operations field is open for applications.

We invite applications for the Clinical Research Associate:
On-Site Monitoring & Coordination position located in Denver, CO, United States.

The following position is for a Clinical Research Associate:
On-Site Monitoring & Coordination with IQVIA Inc.

Our team is growing, and we are hiring a Clinical Research Associate:
On-Site Monitoring & Coordination in Denver, CO, United States.