Clinical Research Coordinator - Stroke Center (LA)

Veterans in Healthcare; Los Angeles (CA); On-site; USD 43,000 - 68,000; Full time

Job summary

UCLA Health in Los Angeles, CA is seeking a Clinical Research Coordinator to support the Stroke Center’s clinical studies. You will oversee tasks from study setup through conduct and closeout, ensuring adherence to protocols, FDA regulations, and ICH Good Clinical Practice.

This role involves coordinating with the Principal Investigator, regulatory staff, sponsors, and other sites to manage regulatory compliance, study logistics, and timely, high‑quality data collection.

Qualifications

• Requires coordination of clinical studies and regulatory compliance.
• Familiarity with FDA regulations and ICH GCP guidelines preferred.
• Ability to manage study setup, conduct, and closeout processes.

Responsibilities

• Oversee tasks from study setup through conduct and closeout.
• Ensure adherence to study protocols and regulatory policies.
• Collaborate with PI, sponsors, and departments to support study administration.

Skills

Regulatory compliance

Study coordination

Clinical monitoring

Cross-functional collaboration

Job description

UCLA Health in Los Angeles, CA is seeking a Clinical Research Coordinator to support the Stroke Center’s clinical studies. You will oversee tasks from study setup through conduct and closeout, ensuring adherence to protocols, FDA regulations, and ICH Good Clinical Practice.

This role involves coordinating with the Principal Investigator, regulatory staff, sponsors, and other sites to manage regulatory compliance, study logistics, and timely, high‑quality data collection.