Research Compliance Coordinator III

Description
The Tulane Human Research Protection Office (HRPO) administers the University's Human Research Protection Program (HRPP) and Institutional Review Boards (IRBs), which are charged with reviewing and monitoring human subjects' research under the auspices of the University. The employee in this position participates in all aspects of IRB communication and database management, paper and electronic file management, meeting preparation and post meeting activities. The employee supports the research community with IRB protocol submissions and the use of IRB forms.





Responsibilities



Qualifications
Minimum Qualification:




Bachelor's degree and two years of experience related to IRB issues and human subjects research protection, ethics, clinical trial performance, industry, and/or experience in a clinical field/setting






OR




High School or equivalent with 6 years of related experience


Preferred Qualification:




Certified IRB Professional (CIP certification is highly desirable or will be required once eligible)