**Description**

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Summary:
Conducts studies as outlined by protocol, educating patients and families, ensuring compliance, and following all established protocols and guidelines.

Responsibilities:
1. Reviews research protocols to determine availability of resources, subjects and equipment needs.
2. Educates patients and families about clinical trials, potential benefits and goals of clinical research. Communicates to physicians and other staff concerning protocols that are open to enrollment
3. Obtains written informed consent with appropriate HIPAA authorization from each patient prior to study enrollment.
4. Conducts study as outlined by protocol. Follows established guidelines in the collection of data. Ensures regulatory compliance for each study by following IRB policies ...