Senior Clinical Research Associate

Senior Clinical Research Associate for oncology trials at ICON, a large functional services provider. The role involves site management, remote and on-site monitoring, regulatory compliance, and relationship management across multiple Texas locations.

Responsibilities

• Conduct remote and on-site monitoring visits including qualification, initiation, interim, and close-out activities
• Serve as primary contact between sponsor and clinical sites to facilitate trial communications
• Manage site essential documents, TMF reconciliation, and IRB/EC submission support
• Develop and implement corrective and preventive action plans based on identified site issues
• Train site staff on protocol compliance, SOPs, GCP, and regulatory requirements

Requirements

• Bachelor's degree in scientific field preferred
• 5+ years independent clinical trial monitoring with on-site and remote visits
• 2+ years solid tumor clinical trial monitoring experience
• 1+ years early development or Phase I/III oncology trial experience
• Expertise in GxP regulations and oncology monitoring techniques including risk-based approaches
• Veeva systems experience highly preferred
• Willing to travel up to 50%