Senior Oncology CRA: Site Lead & Monitoring

KCR Placement; Miami (FL); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

Employee Assistance Program (LifeWorks

Life assurance

Flexible country-specific benefits

Job summary

ICON Strategic Solutions in Miami/South Florida seeks a Senior Clinical Research Associate with oncology expertise to support sponsor trials. You will monitor sites, ensure data integrity and patient safety across remote and on-site visits, and collaborate with site teams to drive trial success.

Responsibilities include QA oversight, training, CAPA development, IRB submissions, and supporting regulatory inspections. Expect travel up to 50% as needed.

Qualifications

• Bachelor’s degree in a scientific field is preferred.
• 5+ years monitoring clinical trials with on-site and remote visits.
• 1+ years in oncology trials (solid tumors) recommended.
• Experience with regulatory inspections and site staff training.
• Experience in Veeva systems is highly preferred.

Responsibilities

• Perform site management activities and ensure inspection readiness.
• Serve as main liaison between the client’s clinical trial team and sites.
• Conduct remote and on-site monitoring visits to ensure data integrity and patient safety.
• Provide oversight to assess monitoring quality, train staff, and mentor junior CRAs.
• Document monitoring activities and submit visit reports promptly.
• Manage site essential documents and TMF reconciliation.
• Support IRB/EC submissions and approvals.

Skills

Monitoring clinical trials

On-site monitoring

Remote monitoring

GxP and Oncology monitoring

Risk-Based Monitoring

Veeva systems

Site management

CAPA

Education

Bachelor’s degree (scientific field preferred)

Tools

Veeva systems

Job description

ICON Strategic Solutions in Miami/South Florida seeks a Senior Clinical Research Associate with oncology expertise to support sponsor trials. You will monitor sites, ensure data integrity and patient safety across remote and on-site visits, and collaborate with site teams to drive trial success.

Responsibilities include QA oversight, training, CAPA development, IRB submissions, and supporting regulatory inspections. Expect travel up to 50% as needed.