Clinical Research Associate (CRA)

Responsibilities of the Clinical Research Associate

• Conduct site qualification, initiation, interim monitoring, and close-out visits for oncology clinical trials.
• Ensure clinical trial activities are conducted in compliance with ICH-GCP, FDA regulations, and study protocols.
• Review and verify source data, case report forms (CRFs), and regulatory documentation for accuracy and completeness.
• Identify, document, and follow up on site issues, protocol deviations, and corrective action plans.
• Serve as the primary point of contact for investigative sites, providing ongoing training and support.
• Collaborate with cross-functional teams including Clinical Operations, Data Management, and Project Management.
• Prepare detailed monitoring visit reports and maintain accurate trial documentation.

Qualifications of the Clinical Research Associate

• 3+ years of experience as a Clinical Research Associate monitoring interventional clinical trials.
• Direct oncology trial monitoring experience is required.
• Strong knowledge of ICH-GCP guidelines, FDA regulations, and clinical research best practices.
• Experience conducting remote and on-site monitoring visits independently.
• Excellent organizational, communication, and problem-solving skills.
• Ability to travel occasionally to investigative sites as required.
• Must be located in the West Coast or Central time zone.

Compensation for the Clinical Research Associate includes:

• Salary range: $155,000 -- $175,000 depending on experience
• Comprehensive benefits package including medical, dental, vision, 401(k), and PTO
• Fully remote work environment with occasional travel

This job opens for applications on 04/20/2026. Applications for this job will be accepted for at least 30 days from the posting date.