Senior Clinical Trial Coordinator
Há 7 dias
Clinical Research Associates play a vital role in advancing medical knowledge and improving patient outcomes. At ICON, we're committed to providing an inclusive and accessible environment for all candidates.
We're seeking a skilled Clinical Research Associate to join our team, who can work independently and actively to coordinate activities to set up and monitor a study. This includes completing accurate study status reports and maintaining study documentation.
The ideal candidate will have 18 months+ of monitoring experience in phase I-III trials as a CRA, with knowledge of ICH GCP guidelines and expertise to review and evaluate medical data. You will also possess excellent written and verbal communication skills in English, with the ability to produce accurate work to tight deadlines within a pressurized environment.
This role requires frequent travel, with at least 60% of the time spent on international and domestic assignments. A valid driving license is essential, as you will be required to drive when necessary.
We offer a comprehensive benefits package, including a competitive salary, annual bonuses, and a range of health insurance options. Our goal is to provide a supportive and inclusive work environment that allows you to thrive and grow in your career.
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