Ohio Licensed Regulatory Manager

Job Summary

A company is looking for a Regulatory Manager for the Clinical Trials Office.

Key Responsibilities

• Ensure compliance of clinical research protocols with university, state, and federal regulations
• Serve as the primary contact for IRB submissions and manage the development of submission packets
• Oversee regulatory updates, training needs, and conduct internal audits to ensure compliance

Required Qualifications

• Bachelor's Degree in biological sciences, health sciences, social sciences, or a related medical field
• 5 years of experience in a clinical research or administrative role
• Knowledge of clinical research regulations and compliance requirements
• ACRP or SOCRA certification is required
• Master's degree in a relevant field is preferred