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Johns Hopkins UniversityNew
Overview
The coordinator manages the administrative and logistical implementation of clinical research protocols to ensure validity of findings. Key duties include participant recruitment, consenting, data collection, and coordinating with the Institutional Review Board.
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Compensation
$17 - $30 / HOUR
Posted
New
Johns Hopkins University
The coordinator will administratively manage clinical protocol implementation and ensure the efficient logistical execution of study activities. Key duties include recruiting participants, managing the consenting process, and handling IRB submissions and data collection.
16 days ago
The coordinator will administratively manage clinical protocol implementation and ensure the logistical efficiency of study activities. Key duties include recruiting participants, managing the consenting process, and handling IRB submissions and data collection.
The Clinical Research Coordinator will manage the logistical implementation of clinical protocols and ensure adherence to study activities. They will also provide administrative support for regulatory issues, including IRB submissions and participant recruitment.
1 month ago
Medpace, Inc.
The Study Start-Up Coordinator will communicate with research sites to collect essential documents for clinical trials and maintain quality reviews of trial documents. They will also manage timelines for study start-up and develop solutions to regulatory challenges.
Salary not listed
2 months ago
The coordinator will administratively manage the implementation of a clinical research protocol, ensuring efficient logistical execution and providing administrative support for regulatory matters. Key duties include coordinating all study activities to maintain protocol adherence and data validity, assisting personnel, managing participant recruitment and consenting, and handling data entry and IRB submissions.
The coordinator will administratively manage the implementation of a clinical research protocol, ensuring efficient logistical execution and providing administrative support for regulatory matters related to the study.
