IRB Full Board Coordinator: Regulatory Support (Hybrid)

University of Iowa; Iowa City (IA); Hybrid; USD 43,000 - 53,000; Full time

Job summary

The University of Iowa is seeking an IRB Full Board Coordinator to provide administrative support and regulatory guidance for human subjects protection programs. You will coordinate activities among UI IRBs, committees, and investigators in a hybrid Iowa-based role.

Responsibilities include guiding applicants through the IRB process, ensuring compliance with federal regulations, and attending meetings to document regulatory determinations.

Qualifications

• Bachelor’s degree in an appropriate field or equivalent combination of education and experience.
• Ability to learn and apply federal regulations, policies, and IRB requirements for human subjects research.
• Proven skill in managing multiple priorities with accuracy and attention to detail.
• Strong collaboration, communication, and customer-focused service orientation.
• Ability to listen to feedback and provide clear written communications.
• Experience with IRB submissions and regulatory correspondences is desirable.

Responsibilities

• Coordinate activities and interactions among UI IRBs, committees, and investigators.
• Guide applicants through the IRB application process and ensure regulatory compliance.
• Attend IRB meetings to document regulatory determinations when needed.

Skills

Regulatory knowledge

Problem solving

Organizational skills

Communication

Active listening

Written communication

Education

Bachelor's degree

Tools

Electronic research database

Electronic workflow system

Job description

The University of Iowa is seeking an IRB Full Board Coordinator to provide administrative support and regulatory guidance for human subjects protection programs. You will coordinate activities among UI IRBs, committees, and investigators in a hybrid Iowa-based role.

Responsibilities include guiding applicants through the IRB process, ensuring compliance with federal regulations, and attending meetings to document regulatory determinations.