Senior Oncology CRA - Remote & On-Site Monitoring Lead

ICON Strategic Solutions; Texas; On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Health insurance

Retirement plan

Life assurance

Job summary

ICON Strategic Solutions in Texas is seeking a Senior Clinical Research Associate (Oncology) to manage site relationships and monitor sponsor-dedicated trials. The role combines on-site and remote monitoring to uphold data integrity and patient safety within oncology programs.

You will support IRB submissions, drive site feasibility and activation, and ensure inspection readiness across trials. Travel up to 50% is required, and collaboration with cross-functional teams will be essential for

Qualifications

• Bachelor’s degree in a scientific field.
• 5+ years of monitoring clinical trials independently (on-site and remote).
• At least 2 years monitoring solid tumor clinical trials.
• 1+ years oncology early development trial experience or Phase I/III Oncology trials.
• Solid tumor monitoring and GxP expertise; willingness to travel 50%.

Responsibilities

• Perform site management to support Oncology site success and inspection readiness.
• Act as primary contact between client trial team and sites to facilitate communications.
• Conduct remote and on-site monitoring visits to ensure data integrity and patient safety.
• Document monitoring activities and submit visit reports in a timely manner.
• Support IRB/EC submissions and regulatory approvals at sites.
• Review KRIs and drive CAPA plans to resolve issues.
• Lead site engagement and activation activities; train site staff as needed.

Skills

Oncology monitoring

Veeva experience

Site relationship management

Risk-Based Monitoring

Regulatory inspections support

Travel up to 50%

Education

Bachelor’s degree (scientific field preferred)

Tools

Veeva systems

Job description

ICON Strategic Solutions in Texas is seeking a Senior Clinical Research Associate (Oncology) to manage site relationships and monitor sponsor-dedicated trials. The role combines on-site and remote monitoring to uphold data integrity and patient safety within oncology programs.

You will support IRB submissions, drive site feasibility and activation, and ensure inspection readiness across trials. Travel up to 50% is required, and collaboration with cross-functional teams will be essential for