Job Description

IQVIA MedTech seeks a Clinical Research Associate II to conduct site monitoring and management for medical device and diagnostic studies. The role ensures protocol compliance, regulatory adherence, and data integrity across assigned clinical trial sites.

Responsibilities

• Conduct site monitoring visits including initiation, ongoing monitoring, and close-out according to protocol and regulatory standards
• Partner with sites on subject recruitment planning and tracking to meet enrollment targets
• Deliver protocol training and maintain regular communication with sites regarding compliance and expectations
• Evaluate site practices for protocol adherence and data quality; escalate issues as needed
• Track study progress including regulatory approvals, enrollment metrics, CRF completion, and data queries

Requirements

• Bachelor's degree in scientific or healthcare discipline preferred
• Minimum 1 year of on-site clinical trial monitoring experience
• Strong knowledge of GCP and ICH guidelines
• Proficiency with Microsoft Office and laptop/mobile devices
• Excellent written and verbal English communication skills
• Strong organizational and problem-solving abilities

Compensation: $90,200-$150,400 base

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