ICON, a leading Clinical Research Organization, is seeking passionate, resilient and inspiring Graduates to join our team as a Clinical Trial Assistant. This opportunity offers an entry-level permanent position to highly skilled individuals interested in a career in clinical research.
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.
ICON is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.
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Salary
Location
Chile, Santiago
Location
Santiago
Remote Working
Office or Home
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc. As a key member of our research department, you will be responsible for overseeing and coordina
Reference
JR139624
Expiry date
01/01/0001
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