Clinical Research Analyst — IRB/FDA Submissions Lead
Providence
Providence Swedish is seeking a Regulatory Coordinator to prepare, facilitate, coordinate, and submit documentation required by federal, state, and local regulations related to research conduct. You will lead Research Assistants, provide on-the-job training, and manage priorities to support project objectives and ensure protection of human subjects. Responsibilities include coordinating IRB submissions, FDA-related filings, and other regulatory documents, with a focus on compliance and timely #J-18808-Ljbffr Providence
Vacancy posted 1 day ago
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