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JR066622

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.

List #1

Day in the life

Headshot of male
Leading Through Change: Zhong Yao's Journey at ICON in China

Teaser label

Our People

Content type

Blogs

Publish 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

From culture to collaboration, Zhong Yao explains how ICON China delivers quality clinical trials, and empowers local talent.

Read more
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How Data Moves Through a Clinical Trial

Teaser label

Industry

Content type

Blogs

Publish 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

Discover how data flows through a clinical trial and learn where your skills could fit within clinical research.

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Male and female auditing a manufacturing facility
Quality and Compliance - A Plain Language Guide

Teaser label

Industry

Content type

Blogs

Publish 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

Teaser label

A clear, practical introduction to quality and compliance for those starting a career in clinical research.

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