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LCMC Health
Overview
The role manages regulatory documents and submissions to pharmaceutical sponsors, IRBs, and CROs to implement clinical trials. It also involves coordinating audits, performing quality assurance, and mentoring junior staff members.
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Compensation
Salary not listed
Posted
8 days ago
OneOncology
The Research Regulatory Coordinator manages regulatory files, IRB submissions, and essential documentation for clinical trials. They coordinate with sponsors and investigators to ensure compliance with regulatory best practices and safety reporting.
16 days ago
