CRA: Clinical Trials Monitoring & Data

ICON

ICON is looking for a Clinical Research Associate in St. Louis who will play an essential role in clinical trials, ensuring protocol compliance and data integrity. The successful candidate will conduct visits, prepare study documentation, and collaborate with site staff. A Bachelor’s degree in a scientific or healthcare-related field and at least 9 months of monitoring experience are essential. ICON values inclusion and offers competitive health insurance, retirement plans, and additional benefits to support work-life balance. #J-18808-Ljbffr

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Vacancy posted 1 day ago

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