Job Description

IQVIA seeks a Clinical Research Associate to conduct site monitoring and management for clinical studies. The role ensures sites comply with protocols, regulations, and sponsor requirements while managing recruitment, data quality, and study documentation.

Responsibilities

• Conduct site monitoring visits including initiation, ongoing monitoring, and close-out activities
• Coordinate subject recruitment planning and tracking with assigned study sites
• Deliver protocol training and maintain regular communication with sites regarding project expectations
• Evaluate site compliance with protocol and regulatory requirements; escalate quality issues
• Track study progress including regulatory submissions, enrollment, CRF completion, and data query resolution

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 Suite and laptop/mobile devices
• Excellent written and verbal English communication skills
• Strong organizational and problem-solving abilities

Compensation: $74,500–$175,100 base annual salary

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