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Working under the direct supervision of Principal Investigator, the Clinical Research Coordinator will be involved in the consenting, obtaining measurements of arm and leg volumes, and the collection, processing, analysis and storage of human biological material. In addition, health related information for research will be collected. A standardized participant recruiting protocol and informed consent of potential participants will be maintained This position will also assists with banking of samples in the general area of lymphatic disorders as well as general operations and procedures of the research laboratory.
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