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Gastroenterology Associates of the Piedmont
Overview
The Research Coordinator manages clinical research activities and ensures compliance with FDA, IRB, and GCP requirements. Key duties include maintaining study documentation, preparing IRB applications, and coordinating between investigators, sponsors, and participants.
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Compensation
Salary not listed
Posted
2 days ago
Piedmont HealthCare PA
Coordinates and supports clinical sites in planning and executing multiple phase clinical trials. Responsibilities include managing regulatory documents, recruiting participants, and collecting study data according to protocols.
4 days ago
UVA Health
The coordinator manages clinical trial conduct, including regulatory documentation, IRB submissions, and patient recruitment and enrollment. They are also responsible for specimen processing, study billing reconciliation, and communicating with sponsors and CROs.
9 days ago
Beth Israel Lahey Health
The Clinical Research Coordinator manages the administration of multiple research studies, ensuring protocol adherence and regulatory compliance. Key duties include recruiting and screening participants, collecting study data, and maintaining communication with sponsors and investigators.
$19 - $31 / HOUR
1 month ago
University of Virginia
This role involves coordinating and implementing clinical trial research studies, working closely with Principal Investigators on all assigned projects, which includes managing recruitment, obtaining informed consent, and overseeing ongoing study conduct activities. Responsibilities also cover preparing and submitting all necessary regulatory documentation to the IRB, managing study billing reconciliation, and ensuring effective communication with study Sponsors.
2 months ago
Imricor Medical Systems Inc
The Senior Clinical Research Specialist will manage clinical research across all project stages, including design, implementation, and execution for one or multiple global clinical studies at all phases. This role involves collecting, analyzing, and reporting accurate trial data while ensuring compliance with Quality System requirements.
$105,000 - $147,000 / YEAR
3 months ago
Trusted Practice Solutions
The Clinical Research Specialist oversees daily regulatory activities related to research studies and coordinates administrative and protocol support services, ensuring studies comply with all applicable regulations and guidelines. This role involves corresponding with sponsors and CROs, preparing necessary documentation, managing trial agreements, and supporting the successful conduct of assigned clinical studies.
$21 - $24 / HOUR
4 months ago
