Clinical Research Analyst
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Job Description
Clinical Research Analyst reviewing human-subject research submissions for Providence’s healthcare system. Supporting IRB members and ensuring regulatory compliance across Western states.
Responsibilities:
- Process full-board and expedited reviews
- Process adverse events, protocol modifications, informed consent forms, and other study activities
- Analyze and review regulatory submissions and activities related to human subjects research for IRB review
- Provide staff support to IRB members
- Serve as a resource to individuals conducting research within the health system
- Liaise between the IRB and researchers
- Assure compliance with regulatory and institutional requirements
Requirements:
- 4 years experience in a health related field or research, or an equivalent combination of education and experience
- 3 years IRB, regulatory, or research experience
- Preferred: 4 years IRB, regulatory, or research experience
- Preferred: 2 years working with electronic IRB platform
- CIP Certification preferred
Benefits:
- Retirement 401(k) Savings Plan with employer matching
- Health care benefits (medical, dental, vision)
- Life insurance
- Disability insurance
- Paid parental leave
- Vacation and holiday time off
- Time off for health issues
- Voluntary benefits
- Well-being resources
- Inclusive workplace where diversity is valued
- Additional compensation may be available, including shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities
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