Regulatory Specialist I

Job Summary

A company is looking for a Regulatory Specialist I in the Comprehensive Cancer Center.

Key Responsibilities

• Assist with ensuring compliance with regulatory standards and maintain audit-ready documentation
• Support the preparation, submission, and maintenance of study-related regulatory documents and budgets
• Participate in study closure activities and maintain long-term storage records of study documentation

Required Qualifications, Training, and Education

• Bachelor's degree in Education, Public Health, Basic Science, or a relevant clinical discipline
• Two years of research experience in regulatory and/or data management activities for clinical trials
• Master's degree in a relevant discipline preferred
• SOCRA or ACRP Certification preferred
• CITI certification for Human Subject Research must be completed if not already done