Responsibilities:

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.

Qualifications

Education:

Required: Bachelor’s health related degree or equivalent

Experience:

Required: 3 years of experience in research

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Description

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.

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