UCLA Health Santa Monica, CA, USA
Responsibilities The Clinical Research Associate will be responsible for ensuring protocol procedures are completed accurately, safely, and in a timely manner, this includes responsibility for research assessment and patient intervention under the supervision of the Principal Investigator. Additional responsibilities include regulatory compliance, patient recruitment and enrollment, data collection, research chart documentation, quality assurance, report preparation, protocol information dissemination to health care professionals, patients and their family members. You will ensure investigational product is adequately managed and documented. Qualifications Required: • Demonstrated clinical research experience, including working knowledge of good clinical practices for clinical research. • Ability to work in more than one environment, travel to participating hospitals, and attend off site staff meetings, conferences and investigator meetings. • Ability to work...