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