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Cincinnati Children's Hospital Medical Center Logo
Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio

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CHRISTUS Health

San Antonio, Texas

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CHRISTUS Health

Irving, Texas

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MemorialCare Health System

Fountain Valley, California

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Vanderbilt Health

Nashville, Tennessee

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Duke University Health System

Durham, North Carolina

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Duke University Health System

Durham, North Carolina

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CHRISTUS Health

Irving, Texas

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Cincinnati Children's Hospital Medical Center Logo
Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio

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Vanderbilt Health

Nashville, Tennessee

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CHRISTUS Health

Santa Fe, New Mexico

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SCL Health

Lafayette, Colorado

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AdventHealth

Orlando, Florida

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Cincinnati Children's Hospital Medical Center Logo
Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio

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AdventHealth

Shawnee Mission, Kansas

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AdventHealth

Orlando, Florida

Vanderbilt Health Logo
Vanderbilt Health

Nashville, Tennessee

Cincinnati Children's Hospital Medical Center Logo
Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio

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WakeMed Health & Hospitals

Raleigh, North Carolina

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Cook County Health

Chicago, Illinois

Cincinnati Children's Hospital Medical Center Logo
Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio

Cincinnati Children's Hospital Medical Center Logo
Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio

Vanderbilt Health Logo
Vanderbilt Health

Nashville, Tennessee

CHRISTUS Health Logo
CHRISTUS Health

Corpus Christi, Texas

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CLIN RSCH COORD II - Nephrology
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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