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IRB Reliance and Education Manager
Creighton UniversityIRB Reliance and Education Manager managing IRB compliance and education programs at Creighton University in Omaha, NE. Ensuring adherence to regulatory guidelines and leading educational initiatives for researchers.
Posted 7/25/2026full-timeOmaha • New York • 🇺🇸 United StatesMid-LevelSenior💰 $75,000 - $85,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in overseeing IRB reliance policies and ensuring regulatory compliance, with a strong focus on federal regulations and ethical principles governing human subjects research. Capable of developing educational programs and providing consultative support to investigators.
Highest-signal resume keywords
IRB Reliance Policies ManagementHuman Research Protection ProgramsFederal Regulations ComplianceSIRB Reliance WorkflowsAnalytical Problem-Solving
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Regulatory ComplianceReliance Agreement NegotiationReliance Study AnalysisDatabase ManagementEducation Program Development
Soft Skills
Strong Analytical AbilitiesProblem-Solving SkillsPresentation Skills
Tools & Technologies
Electronic IRB Systems
Industry Keywords
Research CompliancePublic HealthHuman Subjects Research45 CFR 46FDA Regulations
About the role
Key responsibilities & impact- Oversee the implementation and management of IRB reliance policies.
- Ensure regulatory compliance with reliance agreements between Creighton University and external research entities.
- Lead the negotiation and execution of reliance agreements.
- Serve as the primary contact for external parties in reliance processes.
- Analyze and assess reliance studies and manage amendments.
- Develop and lead educational offerings for IRB members and researchers.
- Maintain a comprehensive database for all reliance agreements.
- Monitor the effectiveness of reliance agreement processes and implement improvements.
- Provide regulatory support and consultative assistance to investigators.
Requirements
What you’ll need- Bachelor's degree required, Master's or JD preferred, in a relevant field such as research compliance, public health, law, or a scientific discipline.
- 4+ years of direct experience in Human Research Protection Programs, research compliance, or a related regulatory field required.
- Strong understanding of federal regulations and ethical principles governing human subjects research (e.g., 45 CFR 46, FDA regulations).
- Experience with sIRB reliance workflows preferred.
- Building robust education programs is helpful.
- Experience presenting education to various audiences.
- Strong analytical and problem-solving abilities.
- Proficiency with electronic IRB systems.
Benefits
Comp & perks- Health insurance
- Retirement plans
- Paid time off
- Professional development opportunities
- Flexible work arrangements