Clinical Trial Research Associate
IQVIA
IQVIA is seeking an individual to assist in clinical trial activities in compliance with regulations. The role emphasizes adaptability, teamwork, and strong interpersonal skills to support study teams, investigators, and office staff. Key duties include screening and enrolling subjects, scheduling visits, data entry, and ensuring adherence to IRB protocols while maintaining subject safety throughout the study process. #J-18808-Ljbffr IQVIA
Vacancy posted 1 day ago
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