Clinical Research Budget & Regulatory Liaison

UCLA Health

Los Angeles (CA)

À distance

USD 46 000 - 91 000

Plein temps

Il y a 4 jours
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Résumé du poste

UCLA Health in Los Angeles, CA is seeking an experienced Budget Amendment Negotiator to coordinate regulatory aspects of clinical research studies. You will review protocols and prepare, manage and submit internal UCLA requirements, FDA and sponsor documents to ensure timely compliance.

Salary offers are determined by qualifications and experience. The role works with study monitors to collect regulatory documents and maintain compliance with federal, state, and university policies; strong

Qualifications

  • Minimum of 1+ years of experience as a clinical researcher.
  • Ability to communicate professionally and work in a team.
  • Ability to manage competing deadlines while following policies.
  • Analytical skills to assess protocols and regulatory requirements.
  • Attention to detail in a fast-paced environment.
  • Strong organizational skills for file management.
  • Proficiency with Adobe and Microsoft Office, especially Excel.
  • Willingness to learn new software tools and processes.
  • Working knowledge of clinical research concepts, policies, and safety regulations.
  • Familiarity with IRBs and research committees.

Responsabilités

  • Coordinate regulatory documents for studies across units.
  • Review protocols and prepare regulatory submissions and forms.
  • Work with study monitors to collect required documents to ensure timely compliance.
  • Ensure adherence to federal, state and university policies.

Connaissances

Clinical research
Regulatory coordination
Documentation
Excel proficiency
Adobe Suite
MS Office
Communication
Organizational skills
Attention to detail
Team collaboration

Outils

Adobe
Microsoft Office
Excel

Description du poste

UCLA Health in Los Angeles, CA is seeking an experienced Budget Amendment Negotiator to coordinate regulatory aspects of clinical research studies. You will review protocols and prepare, manage and submit internal UCLA requirements, FDA and sponsor documents to ensure timely compliance.

Salary offers are determined by qualifications and experience. The role works with study monitors to collect regulatory documents and maintain compliance with federal, state, and university policies; strong

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