This position coordinates regulatory activities for clinical research studies across assigned units, departments, or divisions
Job Summary
This position coordinates regulatory activities for clinical research studies across assigned units, departments, or divisions.
The incumbent conducts detailed reviews of clinical research protocols and prepares required regulatory documents to meet UCLA, FDA, and sponsor requirements.
The role works closely with study monitors to maintain regulatory documentation ensuring timely submissions and full compliance with all applicable regulations.
Matching Summary
This position coordinates regulatory activities for clinical research studies across assigned units, departments, or divisions.
Salary
Base: $31.51 - $62.64 per hour; Budgeted range: $31.51 - $36.00 per hour; Benefits: Not specified
Skills & Requirements
Must-have
clinical research protocol review
regulatory document submission
FDA and IRB compliance knowledge
Adobe and Microsoft Excel proficiency
interpersonal communication skills
Nice-to-have
team collaboration experience
independent task management
experience with external sponsors
Key Requirements
Minimum 1+ years of clinical researcher experience
Working knowledge of human safety protection regulations