Note: The job is a remote job and is open to candidates in USA. Providence is a comprehensive health care organization seeking a Clinical Research Analyst to support its Human Research Protection Program. The role reviews human subjects research submissions and activities for Institutional Review Board compliance, supports IRB members, and serves as a liaison between researchers and the IRB.
Responsibilities
- The HRPP Analyst processes full-board and expedited reviews, adverse events, protocol modifications, informed consent forms, and other study activities
- As an IRB journey-level expert, this position serves as a resource to individuals conducting research within the health system
- The HRPP Analyst is responsible for analyzing and reviewing regulatory submissions and activities related to human subjects research submitted for Institutional Review Board (IRB) review, and providing staff support to the IRB members
- The HRPP Analyst also serves as liaison between the IRB and researchers to assure compliance with regulatory and institutional requirements
Skills
- 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
- 4 years IRB, regulatory, or research experience
- 2 years working with electronic IRB platform
- CIP Certification
Benefits
- Additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities.
- A retirement 401(k) Savings Plan with employer matching
- Health care benefits (medical, dental, vision)
- Life insurance
- Disability insurance
- Time off benefits (paid parental leave, vacations, holidays, health issues)
- Voluntary benefits
- Well-being resources
- Remote workplace arrangement
Company Overview
Company H1B Sponsorship