Site Monitoring Specialist — Clinical Research
Listed on 2026-10-18
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Research/Development
Clinical Research, Research Scientist
IQVIA is seeking a Clinical Research Associate to perform site monitoring and management to ensure sites conduct studies per protocol and regulatory requirements.
Responsibilities include on-site visits, site training, coordinating recruitment plans, tracking regulatory submissions, TMF/ISF maintenance, and collaboration with study teams. Candidates should have a BA/BS in a scientific field and at least 2 years of CRA experience in CRO/sponsor settings, with strong English and MS Office skills.
We are seeking a motivated Site Monitoring Specialist — Clinical Research to join IQVIA in Belmar, NJ, United States.
For the Site Monitoring Specialist — Clinical Research position at IQVIA, we are reviewing applications now.
Step into the Site Monitoring Specialist — Clinical Research role at IQVIA in Belmar, NJ, United States and grow with us.
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