A global clinical research organization is looking for a Site Administrator to support clinical trials. This role involves coordinating study activities, ensuring compliance with guidelines, and assisting with data entry and participant scheduling. The ideal candidate will have at least 1 year of experience in a clinical setting, a high school diploma, and proficiency in MS Office. Strong organizational skills and attention to detail are essential. This position offers remote work flexibility within the Central or Eastern Time Zone. #J-18808-Ljbffr