Senior Clinical Research Coordinator - CNS Trials

Irvine Clinical Research; Los Angeles (CA); On-site; USD 62,000 - 83,000; Full time

Benefits offered by this job

Health insurance (100% paid)

Paid time off: 3 weeks/year

In-person at LA site

Job summary

Irvine Clinical Research is seeking a dedicated Clinical Research Coordinator for our Inglewood Clinical location in Westside Los Angeles. The CRC II–IV will own complex Phase II/III trials, collaborating with Principal Investigators to ensure data integrity, patient safety, and operational excellence.

Responsibilities include study management, protocol adherence, patient coordination, data entry across eSource/CTMS/EDC, and site readiness for sponsor visits and audits.

Qualifications

• 2 to 4+ years of hands-on experience coordinating industry-sponsored clinical trials.
• Experience in CNS/Neurology or Psychiatry is a strong plus.
• Proficiency with clinical trial systems (CRIO eSource, CTMS) and EDC.

Responsibilities

• Manage Phase II/III trials at site from initiation to closeout.
• Ensure protocol compliance with GCP and FDA regulations.
• Coordinate patient visits and cross-functional appointments.
• Enter and manage data across eSource, EDC, CTMS; resolve queries.
• Perform clinical assessments and ensure data integrity.
• Maintain regulatory documentation and readiness for audits.

Skills

Clinical trial coordination

English communication

Tools

CRIO eSource

CTMS

EDC

Job description

Irvine Clinical Research is seeking a dedicated Clinical Research Coordinator for our Inglewood Clinical location in Westside Los Angeles. The CRC II–IV will own complex Phase II/III trials, collaborating with Principal Investigators to ensure data integrity, patient safety, and operational excellence.

Responsibilities include study management, protocol adherence, patient coordination, data entry across eSource/CTMS/EDC, and site readiness for sponsor visits and audits.