The Sr. Clinical Research Associate (Sr. CRA) willbe responsible forperforming investigative site management and monitoring activities throughout the clinical trial lifecycle. This Sr. CRA role will support the client's Oncology clinical trials to ensure data integrity, subject safety, andinspectionreadiness at the clinical investigative sites.

Responsibilities:

• Perform site management activities to support the client's Oncology site success andmaintaina continuous state of inspection readiness

• Act as the primary contact andfacilitateefficient communications between the the client's clinical trial team and the sites

• Perform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in the client's trials

• May perform oversight activities to assess monitoring quality and train/mentor less experienced CRAs

• Promptly document monitoring activities andsubmit/approve visit reports

• Manage site essential document collection and TMF reconciliation with site files

• Support sites with local Institutional Review Board (IRB)/Ethics Committee (EC) submissions and confirm approvals

• Regularly review site Key Risk Indicator (KRI) metrics,issuesand action items to detect trends and ensure prompt resolution

• Independentlydetermineroot causes and develop/implement site Corrective Action and Preventive Action (CAPA) plans

• Deliver training to ensure sitescomply withthe protocol, Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs)and regulations

• Support sites and the client's regulatory inspections

• Contribute to site identification; drive site feasibility and qualification progress; and support site activation activities

• Lead site engagement initiatives and foster relationships with key Oncology sites and networks

Qualifications

• Bachelor27s degree (scientific field preferred)

• 5+ yearsmonitoringclinical trials independently conducting on-site and remote monitoring visits. Atleast 2 years monitoring solid tumor clinical trials.

• 1+ years early development trial experience

• Solidtumorclinical trial experience is required

• Experience utilizing Veeva systems is highly preferred

• Demonstrated experience developing/maintainingsite relationships and securing compliance

• ExpertiseinGxPsand Oncology monitoring techniques (including Risk-Based Monitoring) and terminology

• Experience collaborating with sites frominitialengagement 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%

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• 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

Benefits may vary depending on role and location.

Visit our to read more about the benefits ICON offers.

Salary Range

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