Regulatory Clinical Research Coordinator – IRB/FDA Submissions
Listed on 2026-10-06
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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. You will lead Research Assistants and ensure IRB and FDA submissions comply with requirements.
Join a team dedicated to patient-focused care and research excellence within a large health system, with strong benefits and a collaborative work environment.
As a Regulatory Clinical Research Coordinator – IRB/FDA Submissions, you will play an important part at Providence Health & Services in Seattle, WA, United States.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Seattle, WA, United States.
This opportunity is part of our work in Bio & Pharmacology & Health.
The advertised compensation is 43.000 - 66.000.
We aim to respond to suitable candidates as soon as possible.
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