Regulatory Assistant

Job Summary

Providing essential support for compliance with research protocols, the full-time Regulatory Assistant in the Clinical Trials Office will assist with regulatory functions, prepare protocol submissions to Institutional Review Boards (IRBs), and maintain regulatory files in a remote environment.

Key responsibilities

• Assist with regulatory functions to support clinical research activities
• Prepare protocol submissions to IRBs and provide updates on submission status
• Maintain regulatory files and assist with data entry in the OnCore electronic database

Required qualifications

• Bachelor's degree in biological sciences, health sciences, or life sciences, or equivalent experience
• Experience in a clinical research capacity is desired
• Proficiency in computer skills, with knowledge of database software applications preferred