IRB Specialist
The IRB Specialist performs thorough review of human subjects' research studies submitted to the Institutional Review Board (IRB) office for the purposes of ensuring compliance to regulatory requirements, clarity of informed consents and completeness of IRB application forms. Works in coordination with investigators and research coordinators to ensure completeness and quality of submissions to IRB Panels for review; and manages database, generates formal letters, and instructs individuals for investigators and coordinators on the IRB process and use of IRB database. Job Duties • Reviews research study submissions prior to IRB review for completeness and compliance to regulatory requirements. • Reviews and edits research study consent forms for completeness, readability and format. • Ensures integrity and security of IRB data. • Provides support to investigators and coordinators in the IRB application process and use of the IRB online submission forms. • Supports departmental goals and seeks opportunities to improve work processes. • Performs other related duties as required. Education • Required - Bachelor's degree. • Preferred - Advanced degree. Work Experience • Required - 2 years of relevant research or IRB experience. Certifications • Required - Certification in IRB by the Council for Certification of IRB Professionals (CCIP) and PRIM&R (Public Responsibility in Medicine & Research). If certification is not currently held, incumbent must obtain certification within 12 months of hire if eligible at time of hire, or within 12 months of becoming eligible to test for certification About Ochsner Health Ochsner Health is a leading nonprofit, integrated healthcare system serving communities across Louisiana, Mississippi and the Gulf South. Founded in 1942, Ochsner is guided by its mission to serve, heal, lead, educate and innovate, and is nationally recognized for clinical excellence, innovation and quality outcomes. As part of its integrated care model, Ochsner Health is deeply committed to advancing medical knowledge through robust clinical research and academic collaboration. Ochsner supports a broad portfolio of investigator-initiated studies and clinical trials across multiple specialties, ensuring research is conducted with the highest standards of scientific integrity, regulatory compliance and patient protection. Through collaboration among clinicians, researchers and regulatory professionals, Ochsner translates discovery into meaningful improvements in patient care while strengthening the health of the communities it serves. Apply tot his job