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University of Rochester
Overview
This role coordinates human subject research activities within the Department of Urology, focusing on screening, consenting subjects, maintaining documentation, and managing data collection according to research protocols. The specialist ensures research activities adhere to institutional policies, IRB requirements, and study protocols while coordinating with the Principal Investigator and other study team members.
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Compensation
$21 - $30 / HOUR
Posted
8 days ago
UHS
The Research Assistant will support Clinical Research Coordinators and Medical Directors by assisting with multiple research activities to ensure protocol efficacy and regulatory compliance, including data management projects as needed. Key duties involve ensuring appropriate patient scheduling according to protocol while maintaining confidentiality, and actively participating in the recruitment of study participants.
Salary not listed
1 month ago
McLaren Health Care
The Clinical Research Coordinator II will provide essential support to the Clinical Trials Office, covering study coordination, data management, and regulatory specialization. Key duties involve ensuring all study requirements and regulations are met and documented according to protocol guidelines.
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The IMA Group
The Audiologist will perform comprehensive hearing tests and conduct audiological evaluations. They will analyze diagnostic tests and prepare medical reports for Veterans applying for service-connected benefits.
5 months ago
Northside Hospital Inc.
The Research Nurse I will provide patient care services for patients enrolled in research protocols approved by the Northside Hospital IRB, involving tasks like registration, data handling, reporting adverse events, and managing records. Major functions encompass roles as a practitioner, researcher, educator, and consultant within the research framework.
