Clinical Research Associate I — Site Monitoring
Fortrea
Fortrea is seeking a Site Monitor/Project Coordinator to manage clinical study sites. You will ensure protocol adherence, informed consent, and data integrity across sites, while liaising with vendors and internal teams. The role requires six months of relevant experience, strong regulatory knowledge, and the ability to travel. A driving license and proficient computer skills are essential. #J-18808-Ljbffr Fortrea
Vacancy posted 2 hours ago
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