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About the role
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- You will need to ensure high levels of accuracy, to manage and maintain clinical study documentation
- Provide support to the project teams by updating the Clinical Trial Management Systems
- Arrange and attend internal and external meetings, helping to produce presentation materials and generate meeting minutes
- Assist in the tracking and distribution of safety reports and coordinate document translations, if required
- Contact external and internal individuals; you will collate relevant study information and assist with study payments
- Previous working knowledge of Word, Excel, Outlook and PowerPoint
- Fluent in English, and the local language for the country you are applying
- Excellent oral and written communication skills, issue management and resolutions skills as
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
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