Senior Oncology CRA — Site Leadership & Monitoring

ICON Strategic Solutions; Miami (FL); On-site; USD 95,000 - 135,000; Full time

Benefits offered by this job

Health insurance

Retirement planning

Life assurance

Global Employee Assistance Programme

Work life balance

Job summary

ICON Strategic Solutions in Miami, FL seeks a Senior Clinical Research Associate specializing in Oncology to support site management and monitoring activities across sponsor relationships. This role requires strong site communication, data integrity focus, and active participation in regulatory processes.

Responsibilities include on-site and remote monitoring, CAPA development, site training, and collaboration with IRBs/ECs.

Qualifications

• Bachelor’s degree in a scientific field is preferred.
• 5+ years monitoring clinical trials with on-site and remote visits.
• 2+ years oncology trial experience (solid tumor).
• Experience with GxP and oncology monitoring techniques.

Responsibilities

• Perform site management to support oncology site success and inspection readiness.
• Act as primary contact between client trial team and sites.
• Perform remote and on-site monitoring visits to ensure data integrity and subject safety.
• Document monitoring activities and submit visit reports.
• Manage site document collection and TMF reconciliation.
• Support IRB/EC submissions and approvals.
• Review KRI metrics and drive CAPA actions.
• Develop CAPA plans and train site staff.
• Lead site engagement and activation activities.

Skills

Oncology monitoring

GxP knowledge

Veeva systems

Site management

Communication with sites

Risk-based monitoring

Training site staff

Education

Bachelor's degree (scientific field preferred)

Tools

Veeva

Job description

ICON Strategic Solutions in Miami, FL seeks a Senior Clinical Research Associate specializing in Oncology to support site management and monitoring activities across sponsor relationships. This role requires strong site communication, data integrity focus, and active participation in regulatory processes.

Responsibilities include on-site and remote monitoring, CAPA development, site training, and collaboration with IRBs/ECs.