Field Clinical Research Associate – Sponsor-Focused Trials

IQVIA is seeking an experienced Clinical Monitoring professional to oversee site visits and ensure protocol adherence across multiple sites in the United States. You will drive recruitment planning and manage regulatory submissions while maintaining high-quality data and documentation.

The role requires strong knowledge of GCP/ICH, excellent communication skills, and the ability to collaborate with sponsors and study teams. On-site positions may vary by location.

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