Senior Clinical Research Associate - Site Monitoring

A global CRO is seeking Clinical Research Associates (CRA) to manage clinical trials at designated sites in Little Rock, Arkansas. The role includes liaising with study sites, ensuring compliance with ICH-GCP guidelines, and performing monitoring visits. Critical skills include excellent attention to detail and effective communication. A Bachelor's degree in a relevant field is required, and proficiency in English is a must. The position requires a willingness to travel nationally and possibly internationally.
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