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University of Maryland Medical System Logo
University of Maryland Medical System

Baltimore, Maryland

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Children's Minnesota Logo
Children's Minnesota

St. Paul, Minnesota

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CHRISTUS Health

Irving, Texas

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Vanderbilt Health

Nashville, Tennessee

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Nemours

Wilmington, Delaware

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Duke University Health System Logo
Duke University Health System

Durham, North Carolina

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AdventHealth

Tampa, Florida

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Duke University Health System Logo
Duke University Health System

Durham, North Carolina

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Vanderbilt Health

Nashville, Tennessee

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Northeast Georgia Health System

Gainesville, Georgia

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CHRISTUS Health Logo
CHRISTUS Health

Tyler, Texas

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Children's Minnesota Logo
Children's Minnesota

MN and WI Remote, Minnesota

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Vanderbilt Health

Nashville, Tennessee

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Vanderbilt Health Logo
Vanderbilt Health

Nashville, Tennessee

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Rush University Medical Center Logo
Rush University Medical Center

Chicago, Illinois

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Vanderbilt Health

Nashville, Tennessee

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Fred Hutchinson Cancer Center

Seattle, Washington

Vanderbilt Health Logo
Vanderbilt Health

Nashville, Tennessee

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Vanderbilt Health Logo
Vanderbilt Health

Nashville, Tennessee

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Fred Hutchinson Cancer Center Logo
Fred Hutchinson Cancer Center

Seattle, Washington

Duke University Health System Logo
Duke University Health System

Raleigh, North Carolina

Duke University Health System Logo
Duke University Health System

Durham, North Carolina

Fred Hutchinson Cancer Center Logo
Fred Hutchinson Cancer Center

Seattle, Washington

Vanderbilt Health Logo
Vanderbilt Health

Nashville, Tennessee

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CLIN RSCH COORD II - Data Entry
DescriptionSUBFUNCTION DEFINITION: The healthcare science that determines the safety and effectiveness (efficacy) of medications, devices, diagnostic products and treatment regimens intended for human use. These may be used for prevention, treatment, diagnosis or for relieving symptoms of a disease. To ensure quality, human subject safety and data integrity of clinical trials conducted within the assigned department.REPRESENTATIVE RESPONSIBILITIES???Study Conduct/ Clinical Research Practice Assist in coordinating studies by preparing personnel and materials, preparation of protocols, informed consents, amendments and other necessary documents for review by the IRB and Sponsor. Assemble lab kits and/or gather supplies. Collect and label sampl


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