IRB Review Analyst – Human Research Protection Office

Job Description: • Attend committee meetings to document meeting actions • Communicate requirements to research team and resolve required actions • Screen research studies for compliance with federal regulations • Serve as liaison between committee members and research team • Compose meeting minutes compliant with regulations • Review responses from investigators and approve protocols • Provide guidance to investigators regarding applications Requirements: • Bachelor’s degree or relevant combination of education and/or experience • Certified IRB Professional (CIP) status required when eligible • Relevant Experience (1 Year) in Clinical Research • Skills: Cooperation, Customer Service, Deadline Management, Decision Making, Detail-Oriented, Good Clinical Practice (GCP), HIPAA, Human Subjects Protections, IRB, Medical Knowledge, Multitasking, Oral Communications, Organizing, Paperless Environments, Positive Thinking, Prioritization, Problem Solving Tools, Regulatory Research, Research Coordination, Researching, Software Applications, Stress Management, Teamwork, Working Independently, Written Communication Benefits: • Up to 22 days of vacation • 10 recognized holidays • Sick time • Competitive health insurance packages • Free Metro transit U-Pass for eligible employees • 403(b) Retirement Savings Plan with university contributions • Wellness challenges, annual health screenings, mental health resources, mindfulness programs • 4 weeks of caregiver leave to bond with a new child • Tuition coverage for employees and their familyApply Now

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