IRB Reliance Coordinator , II or III
Listed on 2026-06-22
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Research/Development
Clinical Research, Regulatory Compliance Specialist, Research Scientist
Working Title
IRB Reliance Coordinator I, II or III
DepartmentRsch Compliance, Integrity, Security-1315
Description Of WorkThe Office of Research and Innovation at the University of Nebraska-Lincoln (UNL) is committed to promoting a culture and environment for success in research, scholarship, creative endeavors, and economic development. Conducting novel and impactful research that generates new knowledge, solves real‑world problems, and enhances lives is among the most fundamental purposes of the institution. UNL Research and Innovation has an opportunity for qualified candidates to apply for an IRB Reliance Coordinator position within the Office of Research Compliance, Integrity and Security at one of three levels:
Coordinator I, II, or III. The IRB Reliance Coordinator performs functions related to the oversight, guidance and direction of the UNL HRPP processes and policies with a particular focus on single IRB (sIRB) reliance agreements‑exempt and expedited‑and full‑board IRB project review. The primary focus of this position is serving as the main point of contact and providing guidance to investigators needing to establish the use of the UNL IRB as a sIRB or rely on an external IRB.
This position will have other duties as assigned related to the review of human subjects protocols. The IRB Reliance Coordinator II and III will also have duties related to the conduct of full board IRB meetings.
As an EO/AA employer, qualified applicants are considered for employment without regard to race, color, ethnicity, national origin, sex, pregnancy, sexual orientation, gender identity, religion, disability, age, genetic information, veteran status, marital status, and/or political affiliation. See:
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Required Qualifications Coordinator I
- Bachelor’s degree plus 1 year of relevant experience at a research university or in a clinical or regulatory environment; equivalent education/experience considered.
- Strong written and verbal communication skills.
- Strong decision‑making, planning, and organizational skills.
- Solid presentation, negotiation, problem‑solving, conflict resolution, and meeting management skills.
- Understanding of policy and procedure interpretation and implementation.
- Demonstrated ability to work in a complex multi‑tasking environment.
- Bachelor’s degree plus 2 years of relevant experience at a research university or in a clinical or regulatory environment; equivalent education/experience considered.
- Outstanding written and verbal communication skills.
- Strong decision‑making, planning, and organizational skills.
- Solid presentation, negotiation, problem‑solving, conflict resolution, and meeting management skills.
- Prior experience with policy and procedure interpretation and implementation.
- Demonstrated ability to work in a complex multi‑tasking environment.
- Bachelor’s degree plus 4 years of relevant experience at a research university or in a clinical or regulatory environment; equivalent education/experience considered.
- Outstanding written and verbal communication skills.
- Strong decision‑making, planning, and organizational skills.
- Solid presentation, negotiation, problem‑solving, conflict resolution, and meeting management skills.
- Prior experience with complex policy and procedure interpretation and implementation.
- Demonstrated ability to work in a complex multi‑tasking environment.
- Bachelor’s degree in a STEM field.
- CITI trained.
- Completion of CIP.
- Bachelor’s degree in a STEM field.
- 4 years of relevant experience at a research university or in a clinical or regulatory environment.
- CITI trained, CIP or CIM certification.
- Master’s degree in a STEM field.
- 6 years of relevant experience at a research university or in a clinical or regulatory environment.
- Decision‑making experience.
- Supervisory experience.
- CITI trained, CIP or CIM certification.
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