CRA II - Oncology - West Coast

As a Clinical Research Associate, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

What You Will Be Doing :

• Manage all aspects of site evaluation, initiation, monitoring, and close-out for 3 studies across 10–12 sites.
• Ensure trial conduct adheres to ICH GCP, FDA regulations, SOPs, and protocol requirements.
• Train and retrain site personnel on study protocols, systems, and operational procedures.
• Monitor and document adverse event and serious adverse event reporting to ensure patient safety.
• Collaborate with sites to develop and execute recruitment strategies to meet enrollment targets.
• Ensure data integrity through EDC oversight, timely query resolution, and support of database lock.
• Maintain audit-ready documentation and reconcile with the Trial Master File.
• Monitor investigational product and non-clinical supply management.
• Identify and resolve site performance, quality, or compliance issues with effective intervention plans.
• Serve as the primary liaison between site personnel and sponsor study teams, ensuring seamless communication and oversight.

You Are :

Pay Range ($91,336 / yr USD – $114,170 / yr USD)

What ICON can offer you :

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include :

Visit our careers website to read more about the benefits of working at ICON :   https : / / careers.iconplc.com / benefits

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

https : / / careers.iconplc.com / reasonable-accommodations

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.