UCLA Health
Laguna Hills, 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...
Employment Type (feed only): |
FULL TIME
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