Sr. CRA - Oncology

ICON Strategic Solutions; Los Angeles (CA); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Competitive base salary

Health and wellbeing programmes

Retirement and pension plans

Learning and development opportunities

Job summary

ICON Strategic Solutions in Los Angeles seeks a Senior Clinical Research Associate specializing in Oncology. The role involves site management and monitoring activities during clinical trials to ensure data integrity and subject safety.

The ideal candidate will have a Bachelor’s degree, over 5 years of independent trial monitoring experience, and familiarity with solid tumors. ICON offers a comprehensive rewards package emphasizing health and career development.

Qualifications

• 5+ years monitoring clinical trials with on-site and remote visits, with solid tumor experience.
• 1+ years early development trial experience required.
• Willingness to travel up to 50%.

Responsibilities

• Perform site management activities for Oncology trials.
• Act as primary contact facilitating communication with trial teams.
• Monitor compliance with protocol, SOPs, and regulations.

Skills

Monitoring clinical trials independently

Veeva systems

GxPs and Oncology monitoring techniques

Developing and maintaining site relationships

Site activation

Education

Bachelor’s degree (scientific field preferred)

Job description

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

Senior Clinical Research Associate - Oncology - Southern California

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

The Sr. Clinical Research Associate (Sr. CRA) will be responsible for performing 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, and inspection readiness at the clinical investigative sites.

Responsibilities

• Perform site management activities to support the client's Oncology site success and maintain a continuous state of inspection readiness
• Act as the primary contact and facilitate efficient communications between 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 and submit/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, issues and action items to detect trends and ensure prompt resolution
• Independently determine root causes and develop/implement site Corrective Action and Preventive Action (CAPA) plans
• Deliver training to ensure sites comply with the 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

• 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 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%

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

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

Benefits

• 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.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.