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University of Colorado
Overview
The specialist manages the operationalization and regulatory startup of clinical research studies, acting as the primary liaison between investigators and sponsors. Responsibilities include drafting regulatory documents, developing budgets, and ensuring compliance with FDA and GCP standards.
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Compensation
$58,705 - $78,665 / YEAR
Posted
11 days ago
Manage the startup process for clinical research studies, including regulatory approvals, budget negotiations, and site activation. Act as the primary liaison between investigators and sponsors while ensuring compliance with FDA and GCP standards.
McLaren Health Care
Provide study coordination, data management, and regulatory support for the Clinical Trials Office. This includes maintaining logs, managing patient data, and coordinating monitoring visits and multidisciplinary meetings.
Salary not listed
16 days ago
Provide coordinator, data management, and regulatory support to the Clinical Trials Office. Manage study requirements, maintain databases, and coordinate site visits and monitoring activities.
The Regulatory Affairs Coordinator independently manages all IRB and regulatory processes for ophthalmology research studies. Responsibilities include preparing regulatory submissions, maintaining investigator site files, and ensuring compliance with institutional and federal regulations.
$59,995 - $87,761 / YEAR
2 months ago
