The IRB Reliance Liaison oversees the submission process for human subjects’ research studies that are conducted under an IRB Authorization/Reliance Agreements in which UT Health Science Center is the relying IRB.
In Short
Oversee submission process for human subjects’ research studies.
Interact with researchers, clinical study sites, and external organizations.
Assist with determining when an IRB authorization/reliance agreement is needed.
Manage local context review.
Process administrative changes to cede applications.
Assist with execution of Individual Investigator Agreements.
Work closely with IRB Reliance Managers.
Address IRB reliance issues.
Ensure compliance with regulatory standards.
Support research initiatives at UT Health Science Center.
Requirements
Experience in human subjects research.
Knowledge of IRB processes and regulations.
Strong communication skills.
Ability to manage multiple projects.
Detail-oriented with strong organizational skills.
Experience working with clinical study sites.
Ability to work independently in a remote setting.
Familiarity with research compliance.
Problem-solving skills.
Team player with collaborative mindset.
Benefits
Fully remote position.
Competitive salary.
Opportunity to work in a dynamic research environment.
Support for professional development.
Collaborative team culture.
Flexible work hours.
Health and wellness benefits.
Access to research resources.
Engagement in meaningful research.
Networking opportunities with professionals in the field.