Job description: Develop management systems and prepare for study initiationReview with the Principal Investigator the inclusion/exclusion criteria, overall structure and requirements of each protocolScreen and enroll study subjectsReview the protocol, Informed Consent Form, and follow-up procedures with potential study subjectsSchedule subjects for follow-up visitsAssist investigators in assessment of subject response to therapyAttend study-related meetings and trainings as appropriateCommunicate regularly with the Principal Investigator, and monitor (and others responsible for the conduct of the research) study-related issues. Record data and study documentationEnsure all required documentation is complete and appropriately filed. Other assigned.
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