Oregon Licensed Clinical Research Analyst
Job Summary
To support research initiatives, the full-time Oregon Licensed Clinical Research Analyst will analyze and review regulatory submissions, manage IRB processes, and serve as a liaison between researchers and the IRB while working remotely.
Key responsibilities:
- Process full-board and expedited reviews, including adverse events and protocol modifications
- Analyze and review submissions related to human subjects research for IRB compliance
- Provide support to IRB members and act as a liaison to ensure regulatory adherence
Required qualifications:
- 4 years of experience in a health-related field or research, or an equivalent combination of education and experience
- 3 years of experience with IRB, regulatory, or research activities
Complete Job Description
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