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Federated Rural Electric Insurance Exchange

Shawnee, Kansas

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American Academy of Otolaryngology-Head and Neck Surgery

Alexandria, Virginia

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Greenwood Genetic Center

Greenwood, South Carolina

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Greystar

United States - Nationwide

Township of Springwater

Minesing, Ontario, Canada

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Union College of Union County, NJ

Cranford, New Jersey

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University of Michigan - Ann Arbor

Ann Arbor, Michigan

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The University of North Carolina at Chapel Hill

Chapel Hill, North Carolina

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The University of North Carolina at Chapel Hill

Chapel Hill, North Carolina

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Veterans Affairs, Veterans Health Administration

West Haven, Connecticut, Connecticut

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University of Minnesota Twin Cities

Minneapolis, Minnesota

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University of Southern California (USC)

San Diego, California

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Accreditation Council for Continuing Medical Education

Chicago

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Veterans Affairs, Veterans Health Administration

Menlo Park, California, California

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New Jersey Department of Health

Trenton, New Jersey

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Veterans Affairs, Veterans Health Administration

Martinez, California, California

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Veterans Affairs, Veterans Health Administration

Mobile, Alabama, Alabama

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Veterans Affairs, Veterans Health Administration

Sioux Falls, South Dakota, South Dakota

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City of Greenville / Greenlink Transit

Greenville, South Carolina

City of Greenville

Greenville, South Carolina

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Murray State University

Murray, Kentucky

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The University of North Carolina at Chapel Hill

Chapel Hill, North Carolina

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University of Michigan - Ann Arbor

Ann Arbor, Michigan

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The Ohio State University

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The Ohio State University

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Clinical Research Specialist 2
Clinical Research Specialist 2 to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the Clinical Trials Office within the Comprehensive Cancer Center.Responsibilities: Assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocolsRecruits, interviews and enrolls patientsEducates respondents of purpose, goals, and processes of clinical studyObtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirementsCoordinates scheduling, conducting, and follow-through of study visits, procedures, & other related tasks in accordance with s


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