Senior Clinical Research Associate

Job Description

What You Will Be Doing :

• Conducting qualification, initiation, monitoring, and close-out visits in accordance with study protocols and ICH-GCP guidelines
• Ensuring the rights, safety, and well-being of study participants are protected
• Verifying the accuracy and completeness of data collected at investigative sites
• Collaborating closely with site staff and cross-functional teams to proactively identify and resolve study-related issues
• Ensuring all study documentation is accurate, up-to-date, and audit-ready
• Providing training and support to site personnel on study procedures and regulatory requirements
• Monitoring complex Phase 1 oncology trials, which may include dose-escalation, first-in-human, and combination therapy protocols
• This is a high-impact role ideal for professionals with strong clinical monitoring skills, a keen eye for detail, and a passion for advancing oncology research at the forefront of innovation.

You Are :

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 :

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.

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.