Senior Cancer Trials Coordinator

University-of-California,-Irvin; Orange (CA); On-site; USD 70,000 - 105,000; Full time

Job summary

UC Irvine is seeking a Senior Clinical Research Coordinator to support cancer center trials across Phase I–IV, ensuring compliance with GCP and regulatory standards. You will coordinate study activities and oversee data management within a dynamic team environment.

You will assist investigators with patient recruitment, prepare regulatory documentation, and maintain OnCore trial information while liaising with sponsors and regulatory bodies to safeguard study integrity and patient safety.

Qualifications

• Bachelor's degree in a related field (e.g., sciences, health).
• Minimum 5–7 years coordinating clinical research.
• Experience with cancer-related research is preferred.

Responsibilities

• Coordinate cancer-related protocols (Phase I–IV) with GCP compliance.
• Attend clinic visits, assist PI with recruitment, and manage regulatory docs.
• Maintain trial data in the trial management system and ensure sponsor communications.

Skills

GCP knowledge

OnCore

Data management

Communication skills

Regulatory knowledge

Team player

Clinical coordination

Education

Bachelor's degree in related field

Tools

OnCore

Job description

UC Irvine is seeking a Senior Clinical Research Coordinator to support cancer center trials across Phase I–IV, ensuring compliance with GCP and regulatory standards. You will coordinate study activities and oversee data management within a dynamic team environment.

You will assist investigators with patient recruitment, prepare regulatory documentation, and maintain OnCore trial information while liaising with sponsors and regulatory bodies to safeguard study integrity and patient safety.