Site Monitoring & Trial Execution Specialist
Listed on 2026-10-07
-
Research/Development
Clinical Research
IQVIA is seeking a site monitor to perform monitoring visits, manage site training, and ensure protocol compliance across trials. The role requires coordinating with sites to drive subject recruitment, track regulatory submissions, and maintain TMF/ISF documents in line with GCP and local regulations.
Ideal candidates will have 2+ years of on-site monitoring experience, a relevant scientific or healthcare degree, and strong English communication skills.
We are looking to fill the Site Monitoring & Trial Execution Specialist position at IQVIA in Mansfield, OH, United States.
The position is based in Mansfield, OH, United States.
This opportunity is part of our work in Bio & Pharmacology & Health.
The advertised compensation is 72..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
(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).