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About the role
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We empower our Clinical Trial Assistants to work with a collaborative and successful team to support our Clinical Trial Management and Project Management teams with operational activities. They provide administrative support to various projects, maintain and track clinical study documentation, coordinate study materials, and collate relevant study information.
This unique opportunity is designed for individuals with a Bachelor's Degree in Life Sciences, strong organizational skills, excellent written and verbal communication, and working knowledge of computer systems including Microsoft Word, Excel, Outlook, and PowerPoint.
We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results.
There is no limit to what you can achieve at ICON. From contributing to the development of life-saving drugs to working in a team of dedicated experts, your work is always valued. Teamwork is actively encouraged! We value commitment to excellence and promote this across every element of our business. Our Clinical Trial Assistants are engaged and motivated to do their best every day.
Working for ICON you will be provided with a comprehensive benefits package including competitive salary, bonus, 401K with employer match, generous PTO and paid holidays.
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish date
12/10/2025
Summary
Zhong Yao's Journey at ICON Plc in China Zhong Yao's career in clinical research spans over two decades, with leadership roles across major CROs and a commitment to advancing healthcare in China.
Teaser label
IndustryContent type
BlogsPublish date
12/01/2025
Summary
How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i
Teaser label
IndustryContent type
BlogsPublish date
11/28/2025
Summary
Quality and Compliance for New Entrants: A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job
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