Base: $31.51 - $62.64 hourly; bonus/equity: not sp...
On-site
Review clinical research protocols in detail
Manage regulatory document submissions
Ensure compliance with fda and university policies
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.
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 in detail
Manage regulatory document submissions
Ensure compliance with FDA and university policies
Nice-to-have
Effective communication with external collaborators
Ability to prioritize competing deadlines
Experience working with IRBs and sponsors
Key Requirements
Bachelor's degree or equivalent combination of education and experience
Minimum of 1+ years of experience as a clinical researcher
Working knowledge of human safety protection regulations and laws