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ICON plc

Senior Clinical Research Associate

ICON plc

. Perform site management activities to support the client's Oncology site success and maintain continuous inspection readiness .

Posted 9/25/2026full-timeRemote • Florida • United StatesSeniorWebsite

About the role

Key responsibilities & impact
  • Perform site management activities to support the client's Oncology site success and maintain continuous inspection readiness
  • Act as the primary contact between the client's clinical trial team and sites
  • Perform remote and on-site monitoring/co-monitoring visits, including Site Qualification, Site Initiation, Interim Monitoring, and Close-Out Visits
  • Perform oversight activities to assess monitoring quality and train or mentor less experienced CRAs
  • Document monitoring activities and submit or approve visit reports
  • Manage site essential document collection and TMF reconciliation with site files
  • Support local IRB/Ethics Committee submissions and confirm approvals
  • Review site KRI metrics, issues, and action items to detect trends and ensure prompt resolution
  • Determine root causes and develop or implement site CAPA plans
  • Deliver training on protocols, SOPs, GCPs, and regulations
  • Support sites and the client's regulatory inspections
  • Contribute to site identification, feasibility, qualification, and activation activities
  • Lead site engagement initiatives and foster relationships with Oncology sites and networks

Requirements

What you’ll need
  • Bachelor’s degree (scientific field preferred)
  • 5+ years monitoring clinical trials independently conducting on-site and remote monitoring visits
  • At least 2 years monitoring solid tumor clinical trials
  • 1+ years early development oncology trial experience and/or Phase III Oncology trial experience
  • Solid tumor clinical trial experience is required
  • Experience utilizing Veeva systems is highly preferred
  • Demonstrated experience developing/maintaining site relationships and securing compliance
  • Expertise in GxPs and Oncology monitoring techniques, including Risk-Based Monitoring, and terminology
  • Experience collaborating with sites from initial engagement through close-out phases
  • Experience activating sites
  • Experience training site staff
  • Experience supporting sites and/or sponsors in regulatory inspections
  • Experience working within a Functional Services or in-house monitoring model is preferred
  • Willing to travel up to 50%
  • Legal right to work in the country where the role is based

Benefits

Comp & perks
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways