CRA II: Site Monitoring, Data Quality & Compliance

ICON

ICON is seeking a Clinical Research Associate in Nashville, Tennessee. The role involves conducting site visits, ensuring compliance, and maintaining data integrity for clinical trials. Candidates must have a Bachelor’s degree in a relevant field and at least 2 years of clinical trial monitoring experience. The position requires strong organizational and communication skills. ICON offers competitive benefits, including health insurance and retirement planning, fostering a diverse and inclusive workplace. #J-18808-Ljbffr

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Vacancy posted 14 hours ago

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