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Avera Health
Overview
Coordinates and implements research study protocols, including participant recruitment, screening, and data collection. Manages laboratory specimens and ensures compliance with FDA regulations and Good Clinical Practices.
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Compensation
$22 - $37 / HOUR
Posted
4 days ago
The Ohio State University
Coordinate and oversee clinical research protocols for hematology malignancies, focusing primarily on observational studies. Responsibilities include managing patient eligibility, obtaining informed consent, ensuring data integrity, and maintaining compliance with IRB and FDA regulations.
Salary not listed
14 days ago
University of Massachusetts Medical School
The Clinical Research Coordinator II will coordinate regulatory activities and manage data collection for complex research protocols. They will also ensure compliance with study protocols and assist with participant interactions and documentation.
$48,000 - $55,000
23 days ago
The Clinical Research Coordinator I is responsible for coordinating regulatory activities and managing data collection for research protocols. This includes obtaining consent from participants, scheduling visits, and ensuring compliance with study protocols.
$40,000 - $48,000
EvergreenHealth
Coordinates the operations of neuroscience research studies, managing patient records, databases, and case report forms. Responsibilities include recruiting subjects, ensuring protocol adherence, and handling IRB submissions and specimen shipping.
1 month ago
Children’s Minnesota
The Clinical Research Coordinator serves as a project manager to coordinate and implement neonatal research studies while ensuring compliance with protocols and regulatory requirements. Responsibilities include managing study activities, preparing regulatory submissions, overseeing data collection, and facilitating communication between investigators and stakeholders.
UCSF
The Clinical Research Coordinator will perform entry-level duties to support and coordinate clinical studies under the supervision of senior staff. They will assist with patient interactions, data collection, and the maintenance of research documentation.
$28 - $46 / HOUR
2 months ago
The Speech Pathologist will assist the Principal Investigator in clinical research focused on the nature and treatment of communication impairments. Responsibilities include conducting observational and language treatment studies and managing data from medical records.
Catholic Health
The Research Coordinator will review and analyze clinical trial protocols while managing clinical data entry and patient records. They will also coordinate study enrollment, monitor compliance, and support interdepartmental research activities.
4 months ago
