Clinical Research Associate: Sponsor-Dedicated Monitoring
Listed on 2026-10-06
-
Research/Development
Clinical Research
IQVIA is seeking an on-site Clinical Research Monitor in New Jersey to ensure sites conduct studies per protocol and regulatory requirements. You will monitor visits, support recruitment plans, and train site staff, maintaining clear communication and documentation.
The role requires at least 2 years of on-site monitoring experience, knowledge of GCP/ICH, and strong organizational and communication skills. This is an on-site position in the US with potential collaboration across teams.
Join us at IQVIA as our next Clinical Research Associate:
Sponsor-Dedicated Monitoring in Camden, NJ, United States.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Camden, NJ, United States.
This opportunity is part of our work in Bio & Pharmacology & Health.
The advertised compensation is 72..
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).