Clinical Research Assistant

As the Clinical Research Assistant, you will perform administrative and clinical duties at research clinics.

• Perform administrative and clinical duties at research clinics
• Perform EKGs
• Assist with collection of required questionnaires
• Facilitate transport of lab collection supplies to designated areas for collection
• Support the research staff in locating patients' research charts for patient visits and data collection
• Prepare research charts for upcoming visits by ensuring current source documents are on the chart, correct labs are ordered, and new version of informed consent forms (ICF) is printed
• Manage phone messages, collect data from existing records as needed for real-time data collection
• Provide assistance to the research staff to ensure research documents are completed in a timely manner
• Ensure there is an adequate stock of office supplies and equipment for all research clinics
• Schedule and coordinate meetings, appointments, and calendars for research program
• Track and assist in obtaining outstanding training for nurses and investigators as needed
• Assist in prioritizing queries based on due date and importance
• Facilitate obtaining signatures on necessary documents including but not limited to adverse event (AE) and RECIST logs
• Fax/scan documents as needed
• Send on/off study correspondence to appropriate persons
• Participate in educational programs and activities
• Attend required meetings
• Complete protocol training for required studies

• A High School Diploma (GED)
• Medical Vocational/Technical training is preferred
• Experiencing performing EKGs is preferred
• Administrative experience is preferred
• Experience in healthcare is preferred

• 401k matching
• Health insurance
• Flight privileges

Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials.