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
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