IRB Analyst II

Saint Louis University; Missouri; On-site; USD 60,000 - 85,000; Full time

Job summary

Saint Louis University is seeking an IRB Analyst II to coordinate daily review activities for research protocols and assist with HRPP compliance. You will process exempt and expedited submissions, coordinate IRB actions, and prepare documentation for approvals.

The role includes QA support, policy updates, and staff training to uphold federal regulations and AAHRPP standards. Applicants should have a bachelor’s degree, CIP certification, and at least two years in human subjects research.

Qualifications

• Bachelor’s degree required; CIP certification preferred.
• Two or more years of experience with human subjects research/IRB processes.
• Experience with audit, QA, or HRPP activities is an asset.

Responsibilities

• Reviews and processes exempt/expedited protocol submissions as an IRB designee.
• Coordinates IRB review processes and prepares actions and revisions.
• Coordinates IRB meetings and documents meeting minutes.
• Assists with QA activities, CAPA, and HRPP form/policy updates.
• Supports training and development within HRPP staff and researchers.

Skills

ICH/GCP guidelines

FDA regulations

HIPAA Privacy Rule

HRPP policies

Analytical skills

Verbal and written communication

Confidentiality

Microsoft Office

Custom database software

Education

Bachelor’s degree

Master’s degree

Tools

Microsoft Office

Custom database software

Job description

## IRB Analyst IIApply: SLU Saint Louis, MO: Full time: Posted Yesterday: 2026-10109**Who is Saint Louis University? Founded in 1818, Saint Louis University is one of the nation’s oldest and most prestigious Catholic universities. SLU, which also has a campus in Madrid, Spain, is recognized for world-class academics, life-changing research, compassionate health care, and a strong commitment to faith and service.****JOB SUMMARY** The IRB Analyst II coordinates the daily activities associated with the processing of research protocols and all facets of protocol review management to assist the Institutional Review Board (IRB) and Human Research Protection Program (HRPP); performs audits and monitoring visits under the IRB’s Quality Assurance Review (QAR) program; assists institutional research educational activities related to human subjects protections; assists with the training of HRPP staff. **PRIMARY JOB RESPONSIBILITIES*** Reviews and processes exempt and expedited protocol submissions as an IRB designee; coordinates the review process of protocol submissions with IRB reviewers and, when deemed necessary, ancillary office reviewers; determines difficulty level of protocol issues and regulatory determinations; prepares protocols for IRB action; delineates revision requirements; reviews investigators’ responses; makes decisions for approval; aid reviewers’ and HRPP Director in approval decisions; processes or administratively withdraws protocols based on established guidelines* Facilitates the review of all central IRBs, external IRBs, and single IRB submissions; reviews HRPP policies/procedures relative to central IRBs, external IRBs, and single IRB submissions to ensure that all SLU workflows and guidelines are followed and meet current federal regulations* Coordinates IRB meetings; prepares agenda and materials to meet distribution deadlines; reviews materials with HRPP Director and Chairs; prepares draft meeting minutes; documents IRB review determinations; monitors existing and new protocols; gathers information and background material in response to inquiries/issues raised and to make approval decisions; responds to requests for information regarding IRB review* Assists with all quality assurance efforts, including PI quality assurance reviews (QAR) and for-cause and noncompliance audits; monitors human subject research protocols for measures of overall compliance; assists with the analysis/summary of results, identification of alternatives for resolution of issues, and development and monitoring of corrective and preventative action plans (CAPA)* Assists with revisions and implementation of HRPP forms, policies, guidelines, and standard operating procedures; assists with development of materials required for attaining and renewing accreditation by the Association for the Accreditation of Human Research Protection Programs (AAHRPP); assists in the development and presentation of training and seminars to faculty, staff, and students pertaining to research issues and institutional review requirements and processes* Serves as liaison to assigned academic units; supports researchers through the IRB process; attends workshops and conferences focused on current issues affecting the IRB oversight of the protection of human subjects in research; informs Director of issues raised by the IRB or researchers* Assists with the training of HRPP staff, which may include Analysts I, Coordinators, or other support positions; performs internal quality assurance reviews (iQARs) of the work completed by Analysts I and II and provides constructive feedback* Performs other duties as assigned **KNOWLEDGE, SKILLS, AND ABILITIES*** Extensive knowledge of ICH/GCP guidelines, FDA regulations, OHRP regulations, HIPAA Privacy Rule, and HRPP policies and guidelines related to human subject protection, medical and clinical terminology, and research methodology and design* Strong analytical skills with ability to identify issues and solve problems within the framework of federal and state regulations, accreditation standards and institutional requirements* Excellent verbal and written communication skills* Professional demeanor with ability to work both collaboratively and independently, to maintain confidentiality, and to provide excellent customer service* Ability to operate personal computers, Microsoft Office products, and customized data base software* Good organizational skills with ability to work on multiple projects simultaneously* Flexibility and ability to adapt to a changing environment **MINIMUM QUALIFICATIONS*** Bachelor’s degree* Two or more years of current and relevant experience conducting, reviewing, and/or monitoring research involving human subjects* Must hold CIP (Certified IRB Professional) certification **PREFERRED QUALIFICATIONS*** Master's degree**Function**Research SupportScheduled Weekly Hours:40Saint Louis University is an equal opportunity/affirmative action employer. All qualified candidates will receive consideration for the position applied for without regard to race, color, religion, sex, age, national origin, disability, marital status, sexual orientation, military/veteran status, gender identity, or other non-merit factors. If accommodations are needed for completing the application and/or with the interviewing process, please contact Human Resources at 314-977-5847.