Regulatory Coordinator - Radiological Sciences

Uclahealth

Los Angeles, CA, United States
Base: $31.51 - $62.64 hourly; bonus/equity: not sp...
On-site
Review clinical research protocols
Submit regulatory documents to fda
Maintain regulatory documentation files
This role is responsible for coordinating regulatory activities for clinical research studies across assigned units and departments

Job Summary

  • This role is responsible for coordinating regulatory activities for clinical research studies across assigned units and departments.
  • The incumbent reviews clinical research protocols in detail and prepares, manages, and submits all required regulatory documents to meet UCLA, FDA, and sponsor requirements.
  • The position works closely with study monitors to collect, review, and maintain regulatory documentation, ensuring timely submissions and full compliance with federal, state, and university policies.

Matching Summary

This role is responsible for coordinating regulatory activities for clinical research studies across assigned units and departments.

Salary

Base: $31.51 - $62.64 hourly; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Review clinical research protocols
  • Submit regulatory documents to FDA
  • Maintain regulatory documentation files
  • Ensure compliance with federal regulations
  • Collaborate with study monitors

Nice-to-have

  • Effective communication with faculty
  • Ability to work under competing deadlines
  • Experience with external IRBs
  • Team collaboration skills
  • Problem-solving in regulatory context

Key Requirements

  • Bachelor's degree or equivalent experience
  • Minimum of 1+ years as a clinical researcher
  • Working knowledge of human safety protection regulations
  • Experience working with local and external IRBs

Work Rights

Not specified

Tailored Resume

Cover Letter