Clinical Research Regulatory Specialist
Providence Service
Providence Swedish is seeking a Research Coordinator to prepare, coordinate, and submit regulatory documentation for human subjects research, including IRB submissions and FDA-related documents. You will lead Research Assistants, provide training, and align work priorities with project goals.
The role supports compliance with federal, state, and local regulations, ensuring protection of subjects and efficient study operations within the Providence Swedish research ecosystem.
#J-18808-LjbffrVacancy posted 1 day ago
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