Clinical Research Analyst - Remote

About the role

The Human Research Protection Program (HRPP) Analyst processes full-board and expedited reviews, adverse events, protocol modifications, informed consent forms, and other study activities. Serving as an IRB journey-level expert, this position supports individuals conducting research within the health system. The HRPP Analyst analyzes and reviews regulatory submissions and activities related to human subjects research submitted for Institutional Review Board (IRB) review, and provides staff support to the IRB members. Additionally, this role serves as a liaison between the IRB and researchers to ensure compliance with regulatory and institutional requirements.

Responsibilities

• Processes full-board and expedited reviews, adverse events, protocol modifications, informed consent forms, and other study activities
• Serves as an IRB journey-level expert, supporting individuals conducting research within the health system
• Analyzes and reviews regulatory submissions and activities related to human subjects research submitted for IRB review
• Provides staff support to IRB members
• Serves as a liaison between the IRB and researchers to ensure 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 Qualifications

• 4 years IRB, regulatory, or research experience
• 2 years working with electronic IRB platform
• CIP Certification

Skills

Not specified

Benefits

Not specified

Pay

See posting

Schedule

Full time