Clinical Trial Site Management Associate
CurrentEducate and train site and study staff in conduct and management of sponsored studies, including assurance to regulatory and ICH/ GCP compliance. Collected, reviewed, organized clinical trial documents and data to ensure consistency across sites nationally and internationally while maintaining local, regional, and national regulations and compliance. I specialize in study start up, meaning I get trials operational at individual hospitals or clinics. Start-up is a fast paced, deadline driven area requiring impeccable organization, communication, and attention to detail.