Senior Clinical Research Associate
ICON · FL +1 more
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Senior Clinical Research Associate supporting oncology clinical trials in Jacksonville, Florida. Responsible for site management, monitoring visits, data integrity oversight, and regulatory compliance to ensure successful trial execution and subject safety.
What they're looking for
- 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 oncology or Phase I/III trial experience
- Expertise in GCP and oncology monitoring techniques including risk-based monitoring
- Experience developing site relationships, training staff, and supporting regulatory inspections
- Willing to travel up to 50%
What you'll be doing
- Conduct remote and on-site monitoring visits including site qualification, initiation, interim, and close-out activities
- Serve as primary liaison between sponsor and clinical trial sites, facilitating communications and compliance
- Document monitoring activities, manage essential documents, and reconcile trial master files with site records
- Review key risk indicators, identify trends, develop corrective action plans, and deliver protocol training
- Support site identification, feasibility assessment, activation, and engagement with oncology networks
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.