Regulatory Coordinator
The Irvine Clinical Research site network is the largest of its kind on the West Coast. With five research centers in California, we are leaders in the search for new treatments in neurology, psychiatry, and obesity medicine. Our largest area of research is in Alzheimer's Disease prevention and treatment drug trials, and our doctors were the largest contributors in the world to the most recently FDA-approved medication in Alzheimer's Disease.
The Regulatory Coordinator is responsible for managing and maintaining clinical study regulatory documentation in full compliance with IRB, sponsor, and FDA requirements, ensuring all records remain inspection-ready at all times. This role supports study startup, maintenance, and close-out activities while serving as a key liaison between investigators, sponsors, and IRBs.
Job Duties
Job Requirements
$66,500 - $80,000 a year
This is a full-time employment position based in-person at our clinic in the Alzheimer's Orange County building in Irvine. The starting salary for this position is $66,500 - $80,000 per year, depending on experience and education. The company pays for 100% of health / dental / vision individual insurance costs for eligible full-time employees. Vacation (PTO) is earned at a rate of 3 weeks per year.
Regulatory Coordinator • Irvine, CA, United States