Clinical Research Regulatory Specialist
Listed on 2026-10-18
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Healthcare
Clinical Research -
Research/Development
Clinical Research
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.
The following opening is for a Clinical Research Regulatory Specialist with Providence.
Our group is growing, and we are hiring a Clinical Research Regulatory Specialist in Seattle, WA, United States.
This role is for the Clinical Research Regulatory Specialist role at Providence.
We are seeking a motivated Clinical Research Regulatory Specialist to join Providence in Seattle, WA, United States.
Consider building your career as a Clinical Research Regulatory Specialist at Providence.
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