Regulatory Clinical Research Coordinator II

Benefits

Qualifications

• •Candidates should have at least a Bachelor's degree in a relevant field and 2-3 years of regulatory experience in clinical research

Responsibilities

• •The University of Florida is seeking a Regulatory Specialist to serve as a Clinical Research Coordinator II with a focus on regulatory management for clinical trials
• •This role involves coordinating IRB submissions, ensuring compliance with regulations, and supporting study operations