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Sarasota Memorial Health Care System
Overview
Responsible for the timely and accurate administration of regulatory compliance for clinical research, including processing Human Research Protection Program and IRB documentation. The role involves informing leadership and staff regarding the regulatory status of clinical trials.
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Compensation
Salary not listed
Posted
11 days ago
United Urology Group
The Research Coordinator will screen, enroll, and monitor study subjects for clinical trials while ensuring strict adherence to protocols and regulatory standards. Responsibilities include managing study documentation, coordinating with investigators, and performing clinical procedures such as venipuncture and specimen collection.
1 month ago
Flourish Research
The Regulatory Specialist manages and coordinates all regulatory documents and activities for clinical research studies. This includes overseeing submissions to IRBs and sponsors while ensuring compliance with federal regulations and site protocols.
$24 - $29 / HOUR
University of Rochester
The specialist is responsible for the coordination and oversight of regulatory requirements for clinical research protocols. They manage documentation, maintain logs in tracking systems, and act as a liaison between study teams, sponsors, and regulatory committees.
$25 - $35 / HOUR
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.
2 months ago
