Summary

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.

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.

Education

Required: Bachelors health related degree or equivalent

Experience

Required: 3 years experience in research

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Employment practices will not be influenced or affected by an applicant�s or employee�s race, color, religion, sex (including pregnancy), national origin, age, disability, genetic information, sexual orientation, gender identity or expression, veteran status or any other legally protected status. Tenet will make reasonable accommodations for qualified individuals with disabilities unless doing so would result in an undue hardship.