Clinical Research Regulatory Specialist

University of Southern California

Los Angeles, CA, US
Base: $75,968.95 - $101,364.43 annually; bonus/equ...
Experience with irb submissions
Knowledge of fda regulations
Ich-gcp guidelines expertise
The role involves mastering the creation and revision of protocols, informed consents, and case report forms to support principal investigators

Job Summary

  • The role involves mastering the creation and revision of protocols, informed consents, and case report forms to support principal investigators.
  • Candidates must ensure compliance with local, state, and federal regulations including FDA and IRB requirements while maintaining patient confidentiality.
  • This position offers a salary range of $75,968.95 - $101,364.43 within a world-class research university environment.

Matching Summary

The role involves mastering the creation and revision of protocols, informed consents, and case report forms to support principal investigators.

Salary

Base: $75,968.95 - $101,364.43 annually; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Experience with IRB submissions
  • Knowledge of FDA regulations
  • ICH-GCP guidelines expertise
  • Protocol and consent form creation
  • HIPAA compliance knowledge

Nice-to-have

  • Strong problem-solving skills
  • Diplomatic communication abilities
  • Experience in academic settings
  • Training development experience

Key Requirements

  • Bachelor's degree required
  • 2 years combined education/experience
  • Experience with IND/IDE submissions
  • Knowledge of OHRP and DHHS regulations

Work Rights

Not specified

Tailored Resume

Cover Letter