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Kaiser Permanente - Washington Permanente Medical Group Logo
Kaiser Permanente - Washington Permanente Medical Group

Renton, Washington

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Benefis Health System Logo
Benefis Health System

Great Falls, Montana

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Memorial Sloan Kettering Cancer Center

New York, New York

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Benefis Health System

Great Falls, Montana

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Northwest Permanente, Kaiser Permanente Northwest

Portland, Oregon

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Banner Health

Phoenix, Arizona

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Memorial Sloan Kettering Cancer Center Logo
Memorial Sloan Kettering Cancer Center

New York, New York

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Northwest Permanente, Kaiser Permanente Northwest

Portland, Oregon

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Baylor Scott & White Health

Dallas, Texas

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Duke University Health System

Durham, North Carolina

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Banner Health

Scottsdale, Arizona

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Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio

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

Cincinnati, Ohio

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Phoenix Children's Hospital

Phoenix, Arizona

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Stanford Children's Health - Lucile Packard Children's Hospital Logo
Stanford Children's Health - Lucile Packard Children's Hospital

Palo Alto, California

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Valley Children's Healthcare

Madera, California

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St. Luke's Health System

Boise, Idaho

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Banner Health

Scottsdale, Arizona

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Banner Health

Tucson, Arizona

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Memorial Sloan Kettering Cancer Center Logo
Memorial Sloan Kettering Cancer Center

New York, New York

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

Cincinnati, Ohio

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Clinical Research Coordinator II - Communication Sciences Research Center
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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