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OneOncology
Overview
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.
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Compensation
Salary not listed
Posted
16 days ago
K2 Staffing LLC
The Regulatory Associate manages the development and maintenance of regulatory documents for clinical trials, including study start-up, IRB submissions, and ongoing reporting. They also collaborate with clinical operations, sponsors, and IRBs to ensure audit-ready regulatory files and compliance with study protocols.
2 months ago
The Regulatory Associate manages the development and maintenance of regulatory documents for clinical trials, including study start-up, IRB submissions, and close-out procedures. They also collaborate with clinical operations and sponsors to ensure audit-ready regulatory files and compliance with protocol requirements.
