Regulatory Research Assistant

Job Summary

Supporting the regulatory team, the part-time hourly Regulatory Research Assistant will provide administrative assistance, help maintain regulatory files, and support the submission process to Institutional Review Boards (IRBs) while gaining foundational knowledge in clinical research.

Key responsibilities

• Provide administrative and organizational support to regulatory staff
• Assist with preparation, organization, and distribution of study-related documents
• Help maintain regulatory files and electronic systems to ensure records are accurate and audit-ready

Required qualifications

• Bachelor's degree in a scientific, health-related, or administrative field preferred; equivalent experience considered
• Prior experience in clinical research, regulatory affairs, or a related field preferred but not required
• Knowledge of ICH-GCP, FDA, and IRB regulations is desirable
• Exceptional attention to detail and outstanding organizational skills
• Ability to manage multiple tasks simultaneously in a fast-paced environment