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.

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.