Clinical Research Associate: Site Monitor & Study Lead
Listed on 2026-10-13
-
Research/Development
Research Assistant/Associate, Clinical Research, Research Scientist, Biotech Research
IQVIA is seeking an experienced Clinical Research Associate to monitor study sites and ensure data integrity in accordance with GCP and sponsor requirements. You will perform site visits, manage subject recruitment plans, and train site staff while maintaining essential study documentation.
The role requires 2+ years of CRA experience, knowledge of GCP/ICH, and proficiency with EDC/CTMS/eTMF systems. Collaboration with cross-functional teams is essential for successful study delivery.
This role is for the Clinical Research Associate:
Site Monitor & Study Lead role at IQVIA.
This role, Clinical Research Associate:
Site Monitor & Study Lead at IQVIA, could be your next career step.
Are you ready to take on the Clinical Research Associate:
Site Monitor & Study Lead role at IQVIA?
We would love to welcome a new Clinical Research Associate:
Site Monitor & Study Lead to our organisation in Saint Petersburg, FL, United States.
(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).