Clinical Research Coordinator

Principal Duties And Responsibilities

• Assist clinical team in screening potential patients for study participation
• Schedule all protocol required tests and procedures
• Cookordinate patient appointments with physicians, nurses, and all test areas
• Cookordinate and schedule clinical safety laboratory specimen draws and ensure timely results are available to providers
• Prepare pre-visit communication for providers to ensure required assessments are completed and documented
• Maintain point of contact communication with enrolled patients and assist with front line questions regarding study participation
• Develop protocol specific flow charts, intake sheets, and other tools to ensure protocol compliance and proper data acquisition
• Cookordinate, obtain, process, and ship protocol required tissue samples
• Ensure collection, processing (e.g. spin/separate/freeze) and send out of required correlative research blood samples
• Obtain vital signs and perform EKGs as required for individual studies
• Administer quality of life assessments as required for individual studies

Qualifications

• Bachelor's Degree in a related field
• Some relevant research project work, 0-1 year preferred