Job Summary

• The Sr. Regulatory Coordinator plays a key role in providing regulatory oversight and support for multiple federally funded research studies.
• This role contributes to the development and implementation of regulatory and compliance training initiatives within the BTO.
• Coordinates submissions of human subjects research project to the Institutional Review Board (IRB) and of Investigational New Drug Applications (IND’s) to the U.S. Food and Drug Administration (FDA).

Matching Summary

Skills & Requirements

Key Requirements

• Two years Clinical Research Experience
• Bachelor’s degree or equivalent experience
• CCRP certification preferred

Work Rights