Senior Clinical Research Associate

Senior Clinical Research Associate specializing in oncology clinical trials at ICON's sponsor-dedicated model. Role involves site management, remote and on-site monitoring, data integrity oversight, and regulatory support across multiple Texas locations.

Responsibilities

• Conduct remote and on-site monitoring visits including site qualification, initiation, interim, and close-out activities
• Serve as primary contact facilitating communications between sponsor trial team and clinical sites
• Develop and implement corrective and preventive action plans based on identified root causes
• Review key risk indicator metrics and site issues to detect trends and ensure resolution
• Lead site engagement initiatives and support site activation and identification efforts

Requirements

• Bachelor's degree in scientific field
• 5+ years independently conducting on-site and remote monitoring visits
• At least 2 years monitoring solid tumor clinical trials
• 1+ years early development or Phase III oncology trial experience
• Expertise in GxPs, oncology monitoring techniques, and risk-based monitoring
• Experience developing and maintaining site relationships and securing compliance
• Veeva systems experience highly preferred