Research Regulatory Coordinator

Job Summary

A company is looking for a Research Regulatory Coordinator.

Key Responsibilities

• Prepares, completes, and submits required regulatory forms and documents in consultation with the research team
• Manages IRB-deferred studies and maintains communication with external investigators and research teams
• Performs informed consent reviews and modifies consent forms to ensure compliance with institutional guidelines

Required Qualifications, Training, and Education

• Experience in regulatory compliance within clinical research
• Knowledge of IRB and HIPAA guidelines
• Ability to manage multiple projects and maintain detailed documentation
• Familiarity with clinical trial management systems (CTMS)
• Relevant certifications in clinical research or regulatory affairs preferred