(Senior) Clinical Research Associate

IQVIA seeks a Clinical Research Associate to lead site monitoring activities and ensure protocol compliance across clinical trials. The role involves partnering with investigative sites and cross-functional teams to execute studies to GCP/ICH standards while managing regulatory approvals, enrollment tracking, and data quality.

Responsibilities

• Lead and execute site monitoring visits including selection, initiation, routine, and close-out activities
• Build and maintain strong relationships with investigative sites to drive performance and recruitment
• Ensure protocol compliance, data integrity, and high-quality study execution
• Track study progress including regulatory approvals, enrollment metrics, and data quality
• Identify risks, resolve issues, escalate concerns, and maintain accurate documentation

Requirements

• Bachelor's degree in life sciences, healthcare, or related field
• 1.5+ years of on-site monitoring experience
• Solid understanding of GCP, ICH, and regulatory requirements
• Strong communication, problem-solving, and organizational skills
• Ability to manage multiple priorities in fast-paced environment

Compensation: $90,200-$175,100 base