Senior Clinical Research Associate
ICON
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
Vacancy posted 6 days ago
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