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Novo Nordisk

Plainsboro, New Jersey

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Usona Institute

Fitchburg, Wisconsin

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CHRISTUS Health

Corpus Christi, Texas

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CHRISTUS Health

Alamogordo, New Mexico

Northwestern University

Chicago, Illinois

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Fred Hutchinson Cancer Center

Seattle, Washington

Community Blood Center

Kansas City , Missouri

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Baylor Scott & White Health

Dallas, Texas

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AMN Healthcare / Berkshire Health Systems

Pittsfield, Massachusetts

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Human Subjects Protection Specialist
Act as a Clinical Research Ethicist, providing expertise on the implementation of relevant Human Subjects Protection regulations in clinical research. Conduct regulatory and bioethical reviews of clinical trial protocols, including domestic and international sample and site-specific informed consent documents, for compliance with applicable federal regulations and policies. Carry out literature reviews of ethical codes, regulations, and guidance documents relevant to human subjects' protection in clinical research. Train and supervise staff on application of federal regulations. Develop, review, and update informed consent templates, SOPs, and internal guidelines to promote high quality work product.


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