IRB Review Analyst - Human Research Protection Office - Remote

Overview

The IRB Review Analyst will attend committee meetings to document the committee’s actions, communicate requirements to research teams, and ensure compliance with federal regulations and institutional policies.

In Short

• Attend committee meetings and document actions.
• Screen research studies for compliance with federal regulations.
• Serve as a liaison between committee members and research teams.
• Compose meeting minutes compliant with federal regulations.
• Provide guidance to investigators and research staff.
• Maintain knowledge of current regulations and trends.
• Participate in continuing education in human subject research.
• Support coworkers as needed.
• Review and approve research protocols.
• Participate in SWAT! Team activities.

Requirements

• Bachelor’s degree or equivalent experience.
• 1 year of relevant experience.
• Certified IRB Professional (CIP) preferred when eligible.
• Master's degree preferred.
• Strong communication and organizational skills.
• Detail-oriented with good problem-solving abilities.
• Knowledge of HIPAA and GCP.
• Ability to work independently and as part of a team.
• Familiarity with regulatory research.
• Experience in clinical research is a plus.

Benefits

• Up to 22 days of vacation and 10 recognized holidays.
• Competitive health insurance packages.
• Free Metro transit U-Pass for eligible employees.
• Defined contribution retirement savings plan.
• Wellness challenges and mental health resources.
• 4 weeks of caregiver leave.
• Tuition coverage for employees and their families.
• Opportunities for continuing education and conferences.
• Support for work-life balance.
• Inclusive work environment.