Regulatory Coordinator
On-site · Los Angeles, California, United States
Job Summary
Regulatory Coordinator ensures regulatory compliance and Good Clinical Practice (GCP) standards in clinical research. The role manages IRB submissions and oversees studies from initiation through closure, supporting investigators and research staff. Requires a Bachelor1s degree with 3+ years of relevant experience or an associate1s degree with 4+ years of experience, plus experience with an electronic regulatory filing system and current training in human subjects protection, GCP, and HIPAA Privacy. On-site in the Los Angeles, CA area; part-time. Preferred credentials include CCRP/CCRC/SOCRA or equivalent and strong interpersonal, communication, and organizational skills.
Required Qualifications
- Bachelor1s degree with 3+ years of relevant experience OR associate1s degree with 4+ years of experience
- Demonstrated experience with an electronic regulatory filing system
- Current training in human subjects protection education, Good Clinical Practice, and HIPAA Privacy
Desired Qualifications
- Certified Clinical Research Professional (CCRP)
- Certified Clinical Research Coordinator (CCRC)
- SOCRA or equivalent preferred
- Strong interpersonal and client interaction skills
- Strong communication and organization skills
Apply with one swipe on Sorce. We auto-fill applications and apply on your behalf — no cover letters, no 40-minute forms.
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.