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St. Louis University

Jesuit university in St. Louis, MO

IRB Analyst 2

Full-Time
No salary listed
Junior
Bachelor's, Master's
St. Louis, MO, USA
In Person
Academic & Institutional ResearchMedical Research

About the job

Requirements
  • Extensive knowledge of ICH/GCP guidelines, FDA regulations, OHRP regulations, the HIPAA Privacy Rule, HRPP policies and guidelines related to human subject protection, medical and clinical terminology, and research methodology and design.
  • Strong analytical skills and the ability to identify issues and solve problems within federal and state regulations, accreditation standards, and institutional requirements.
  • Ability to operate personal computers, Microsoft Office products, and customized database software.
  • Good organizational skills and the ability to work on multiple projects simultaneously.
  • Bachelor’s degree.
  • Two or more years of current and relevant experience conducting, reviewing, and/or monitoring research involving human subjects.
  • Must hold Certified IRB Professional (CIP) certification.
Responsibilities
  • Review and process exempt and expedited protocol submissions as an IRB designee; coordinate protocol reviews with IRB reviewers and, when needed, ancillary office reviewers; determine issue difficulty and regulatory matters; prepare protocols for IRB action; specify revision requirements; review investigators’ responses; make approval decisions; aid reviewers and the HRPP Director in approval decisions; and process or administratively withdraw protocols according to established guidelines.
  • Facilitate review of central IRB, external IRB, and single IRB submissions; review related HRPP policies and procedures to ensure SLU workflows and guidelines follow current federal regulations.
  • Coordinate IRB meetings; prepare agendas and materials by distribution deadlines; review materials with the HRPP Director and Chairs; prepare draft meeting minutes; document IRB determinations; monitor protocols; gather information and background material for inquiries, issues, and approval decisions; and respond to information requests about IRB review.
  • Assist with quality assurance efforts, including principal investigator quality assurance reviews and for-cause and noncompliance audits; monitor human-subject research protocols for compliance; assist in analyzing and summarizing results, identifying resolution alternatives, and developing and monitoring corrective and preventative action plans.
  • Assist with revisions and implementation of HRPP forms, policies, guidelines, and standard operating procedures; assist in developing materials for AAHRPP accreditation and renewal; and assist in developing and presenting training and seminars for faculty, staff, and students on research issues and institutional review requirements and processes.
  • Serve as liaison to assigned academic units and support researchers through the IRB process; attend workshops and conferences on current issues affecting IRB oversight of human-subject protection; and inform the Director of issues raised by the IRB or researchers.
  • Assist with training HRPP staff, which may include Analysts I, Coordinators, or other support positions; perform internal quality assurance reviews of work completed by Analysts I and II and provide constructive feedback.
  • Perform other duties as assigned.
Desired Qualifications
  • Master’s degree.

About the company

St. Louis University is the database name for Saint Louis University, a private Catholic and Jesuit research university in St. Louis, Missouri. It offers undergraduate, graduate, and professional education and operates an additional campus in Madrid.

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