CTA - Home-based, Seoul, South Korea
As a (CTA) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
What you will be doing:
#LI-remote
#LI-SO1
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: https://careers.iconplc.com/benefitsAt 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-accommodationsInterested 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.
Are you ready to take your career to the next level as a Clinical Trial Associate (CTA) at ICON? We are the world’s largest and most comprehensive clinical research organization, driven by advanced healthcare intelligence. As a CTA, you will play a pivotal role in the management of clinical trials from the comfort of your home in Seoul, South Korea. Your responsibilities will include setting up and maintaining the Trial Master File, coordinating essential documentation, and ensuring everything is in place for smooth EC submissions. You will also be responsible for collecting and updating study trackers and metrics reports, assisting with site contract signatures, and managing payment initiatives. This role is perfect for someone with over two years of CTA experience in CRO or pharmaceutical companies, particularly if you have a background in oncology. We value strong communication skills and a good command of the English language. Join ICON, where we prioritize the welfare and development of our team. You’ll enjoy competitive salary packages, extensive health insurance options, and various benefits focused on your work-life balance. We celebrate diversity and are committed to creating an inclusive environment where everyone can thrive. So if you are looking for an exciting role that combines your passion for clinical research with the flexibility of working from home, we want to hear from you!
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