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Boys Town National Research Hospital

Omaha, Nebraska

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Boys Town National Research Hospital

New Orleans, Louisiana

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Boys Town National Research Hospital

Omaha, Nebraska

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Boys Town National Research Hospital

Omaha, Nebraska

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Boys Town National Research Hospital

Duncan, Nebraska

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Boys Town National Research Hospital

Omaha, Nebraska

Boys Town National Research Hospital Logo
Boys Town National Research Hospital

Omaha, Nebraska

Boys Town National Research Hospital Logo
Boys Town National Research Hospital

Omaha, Nebraska

Boys Town National Research Hospital Logo
Boys Town National Research Hospital

Omaha, Nebraska

Boys Town National Research Hospital Logo
Boys Town National Research Hospital

Portsmouth, Rhode Island

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Boys Town National Research Hospital

Omaha, Nebraska

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Boys Town National Research Hospital

Portsmouth, Rhode Island

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Boys Town National Research Hospital

Carroll, Iowa

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Boys Town National Research Hospital

Omaha, Nebraska

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Sac City, Iowa

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Duncan, Nebraska

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Omaha, Nebraska

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Boys Town National Research Hospital

Omaha, Nebraska

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Boys Town National Research Hospital

Clarinda, Iowa

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West Palm Beach, Florida

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Boys Town National Research Hospital

Omaha, Nebraska

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Boys Town National Research Hospital

Omaha, Nebraska

Boys Town National Research Hospital Logo
Boys Town National Research Hospital

Omaha, Nebraska

Boys Town National Research Hospital Logo
Boys Town National Research Hospital

Omaha, Nebraska

Boys Town National Research Hospital Logo
Boys Town National Research Hospital

Omaha, Nebraska

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Clinical Research Coordinator Bilingual (3-5 Yrs Exp. Required)
This full-time position requires hard working, energetic, experienced research professional available to coordinate the conduct of pharmaceutical sponsored clinical trials from pre-study preparation through closeout visit in accordance with FDA regulations and GCP guidelines. Possess high-level working knowledge and understanding of all assigned protocols, including requirements of patient eligibility, meeting enrollment goals, visit schedule, assessments and lab procedures, phlebotomy, injections, un-blinded coordinator experience, drug accountability, and maintenance of regulatory documents. Facilitate monitor visits and database clean up with sponsor assigned CRAs. Experience preparing CRFs, reviewing and conducting Informed Consent process with subjects, EDC entry and


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