CRA II

Overview

Clinical Research Associate role with ICON Strategic Solutions, working with a world-leading pharmaceutical partner in oncology, cardio-metabolic, vaccines, and related therapeutic areas.

Responsibilities

• Site monitoring from site selection to study close out
• Monitor the progress of assigned clinical trials and escalate protocol deviations, SAEs, or risks to timely completion of study milestones
• Submit monitoring visit reports to the Clinical Trial Manager on time
• Cross-functional collaboration with site staff, PI, CTM, CTA, contracts and SSU team
• Monitoring in global oncology studies, including on-site and remote monitoring visits
• Approx 50% travel, hybrid office-based work

Qualifications

What ICON Can Offer You

ICON’s success depends on the quality of our people. We are committed to a diverse culture that rewards high performance and nurtures talent. In addition to a competitive salary, ICON offers a range of benefits designed to be competitive within each country and focused on well-being and work-life balance for you and your family.

EEO and Accommodation

ICON is committed to an inclusive and accessible environment for all candidates. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If you need a reasonable accommodation for any part of the application process or to perform essential job functions, please contact us through our accommodations page.

Reasonable accommodations :

Note

Interested in the role but unsure if you meet all requirements? We encourage you to apply anyway—there’s a good chance you’re a fit for this or other roles at ICON.

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