Senior Clinical Research Associate
ICON · TX +4 more
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
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.
What they're looking for
- 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%
What you'll be doing
- 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
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.