Sponsor-Dedicated Clinical Research Associate: Site Monitoring
Listed on 2026-10-07
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Research/Development
Research Assistant/Associate, Clinical Research
IQVIA is seeking a Site Monitoring Specialist to ensure study sites conduct the protocol per regulatory requirements. You will perform monitoring visits, manage recruitment, and provide protocol training to sites while maintaining regular communications with investigators.
You will also evaluate site practices against GCP/ICH guidelines, track regulatory submissions and data queries, and support TMF/ISF documentation. This role is based on-site in Durham, NC.
For the Sponsor-Dedicated Clinical Research Associate:
Site Monitoring position at IQVIA, we are reviewing applications now.
We invite applications for the Sponsor-Dedicated Clinical Research Associate:
Site Monitoring position located in Durham, NC, United States.
The following role is for a Sponsor-Dedicated Clinical Research Associate:
Site Monitoring with IQVIA.
Our organisation is growing, and we are hiring a Sponsor-Dedicated Clinical Research Associate:
Site Monitoring in Durham, NC, United States.
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