Sponsor-Aligned Clinical Research Associate; CRA)
Listed on 2026-11-06
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Research/Development
Research Assistant/Associate, Clinical Research, Research Scientist
IQVIA is seeking a Site Monitoring Specialist to oversee monitoring visits, ensure protocol adherence, and maintain study documentation. You will collaborate with sites, track recruitment, and support data quality and regulatory submissions.
The role requires a bachelor’s degree in a scientific or health care field, 1+ year on-site monitoring experience, and strong knowledge of GCP/ICH guidelines, with proficiency in MS Office. Travel may be required.
This opportunity is for the Sponsor-Aligned Clinical Research Associate (CRA) role at Regulatory Jobs.
This role, Sponsor-Aligned Clinical Research Associate (CRA) at Regulatory Jobs, could be your next move.
Are you ready to take on the Sponsor-Aligned Clinical Research Associate (CRA) role at Regulatory Jobs?
We would love to welcome a new Sponsor-Aligned Clinical Research Associate (CRA) to our organisation in Overland Park, KS, United States.
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