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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
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