The job in short
IRB analyst.
Compliance
Details
- Found
- 23 d ago · posted 2026-09-23
- Location as listed
- Albuquerque, NM, US
- Role
- Lab / Clinical Research
- Source
- The company’s own careers site
Full description
The University of New Mexico Office of Research Integrity and Compliance (ORIC) is seeking a highly motivated, detail-oriented individual to join our Office of the Institutional Review Board (OIRB). The OIRB supports IRB members, faculty, staff and students in the administration of the human research protections program (HRPP) on UNM’s Central and Branch Campuses. The office promotes the safety and protection of individuals involved in human research by providing support, guidance, and education to facilitate ethical and scientifically sound research. The IRB Analyst will be primarily responsible for analyzing and reviewing human research proposals for completeness and compliance with federal regulations, IRB guidelines, and institutional policies. Specific Duties Responsibilities Include: Performs administrative analysis of human research submissions to assess completeness, identify potential regulatory and institutional requirements, evaluate compliance with IRB policies and procedures, and identify issues requiring clarification or further review. Applies established IRB procedures and guidance when reviewing submissions and consults with senior analysts or senior IRB staff when additional regulatory or policy guidance is needed. Tracks submissions, requested revisions, investigator responses, and outstanding items to ensure timely processing and appropriate follow-up in accordance with established procedures. Provides guidance and education to investigators, research staff, and students regarding IRB submission requirements and IRB procedures; assists researchers in resolving submission-related questions and deficiencies and consults with senior analysts or senior IRB staff when additional guidance is needed. Prepares and issues IRB correspondence and approval documentation in accordance with established procedures. Reviews investigator responses to IRB questions and requested revisions, evaluates whether requests have been adequately addressed. Identifies any outstanding regulatory or institutional policy items needed based on guidance provided by senior IRB analysts. Composes clear, concise, and detailed correspondence to investigators that clearly communicates committee concerns, questions, and the rationale for requested changes. Assists with preparing meeting agendas, review materials, and related documentation for IRB review meetings; coordinates submission of materials and tracks items requiring follow-up. Coordinates the collection, processing, and recording of IRB records, in accordance with established office procedures. Ensures the accuracy and completeness of IRB records and electronic submission data; identifies and resolves discrepancies and maintains documentation in accordance with institutional recordkeeping requirements.
Lab / Clinical Research jobs in Albuquerque, New Mexico · Lab / Clinical Research jobs in the United States · All Unm jobs