Clinical Research Associate, Sponsor Dedicated

Perform site monitoring visits, manage study site practices, and ensure compliance with clinical trial regulations and sponsor requirements as a Clinical Research Associate at IQVIA.

Requirements

• Bachelor's Degree in scientific discipline or health care preferred
• Requires at least 2 years of year of on-site monitoring experience
• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements

Benefits

• Comprehensive health and welfare benefits
• Incentive plans, bonuses, and/or other forms of compensation
• Professional development opportunities