As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
ResponsibilitiesWhat You Will Be Doing:
Serve as the primary point of contact between investigational sites and the sponsorConduct all types of site visits, including selection, initiation, routine monitoring, and close-outEnsure site compliance with ICH-GCP, SOPs, and regulationsMaintain up-to-date documentation in CTMS and eTMF systemsSupport and track site staff training and maintain compliance recordsMonitor patient safety, ensuring timely and accurate AE/SAE/PQC reportingSupport subject recruitment and retention efforts at the site levelOversee drug accountability and ensure proper storage, return, or destructionResolve data queries and drive timely, high-quality data entryDocument site progress and escalate risks or issues to the clinical teamAssist in tracking site budgets and ensuring timely site payments (as applicable)Collaborating with cross-functional partners including CTAs, LTMs, and CTMs Qualifications
You are:
A graduate with a Bachelor’s degree in Life Sciences or equivalent, or a qualified RNEligible to work in United States without visa sponsorshipA clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industryExperienced across multiple therapeutic areas, ideally including Oncology (Prostate Cancer, and Lung Cancer) and HematologyProficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMFA clear communicator, problem-solver, and collaborative team playerWilling and able to travel up to 50% for on-site monitoring visits across the northeas region, preference given to candidates residing in Ohio to support efficient regional travel
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.