Ensures the accurate progress of clinical trials from initiation through study termination by acting as liaison to Physician, patient, hospital and company or government sponsor.
Ensures all activity is in according with standard operating procedures.
Identify, screen, randomize and enroll patients
Complete all procedures according to IRB approved protocols
Complete documentation
Maintain regulatory documents and assist clinical research operations support team.
Education
Required: Bachelor's degree in a health-related field or equivalent
Experience
Required: 3 years of experience in research
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