Senior Clinical Research Associate
ICON · MO +9 more
Clinical OperationsFull-time$111k–$138kCompany career page
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Senior Clinical Research Associate supporting oncology clinical trials in a sponsor-dedicated model across the South Central region. Responsible for site management, remote and on-site monitoring, data integrity oversight, and regulatory compliance for solid tumor trials.
What they're looking for
- Bachelor's degree in scientific field
- 5+ years independent clinical trial monitoring with on-site and remote visits
- Minimum 2 years solid tumor clinical trial monitoring experience
- 1+ years early development or Phase III oncology trial experience
- Expertise in GxPs, oncology monitoring techniques, and risk-based monitoring
- Demonstrated ability to develop and maintain site relationships and secure compliance
- Veeva systems experience highly preferred
What you'll be doing
- Conduct remote and on-site monitoring visits including site qualification, initiation, interim, and close-out activities
- Serve as primary contact between sponsor clinical trial team and trial sites, facilitating communications
- Develop and implement corrective and preventive action plans based on root cause analysis
- Manage site essential documents, TMF reconciliation, and IRB/Ethics Committee submissions
- Train site staff on protocol, SOPs, GCPs, and regulatory requirements to ensure compliance
Privacy & handoff
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