Clinical Research Coordinator
Current• Facilitated daily clinical trial activities to help conduct studies• Coordinated and balanced multiple studies across a variety of psychiatric indications• Coordinated study protocols under direction of principal investigator• Scheduled, prepared, and performed study visits utilizing source documents• Obtained and processed vitals, ECGs, phlebotomy samples, and other specimen collection as needed• Served as primary point of contact for and ensured safety and well-being of participants• Managed investigational products from pharmaceutical companies and dispensed to participants• Collected, recorded, and managed participant and study• Quality controlled documents and procedures to ensure adherence to protocol criteria • Reviewed medical charts with Principal Investigator to ensure all study criteria are met• Corresponded with pharmaceutical companies regularly to ensure adherence to study standards