UCLA Health Los Angeles, CA, USA
Description The Clinical Research Associate will be responsible for data management of clinical research studies. You will collect and transcribe research patient data and study related information into research records and maintain study patient files. You will work with study monitors to collect accurate data in a timely manner and assist investigators and study coordinators in clinic settings. You may also be responsible for ensuring protocol procedures are completed accurately, safely, and in a timely manner, 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. Work may be assigned by the manager, team leader,...