Senior Clinical Trials Coordinator – Cancer Research

UCI Health Regional Burn Center; Orange (CA); On-site; USD 85,000 - 115,000; Full time

Job summary

UCI Health seeks a Senior Clinical Research Coordinator to support cancer center trials (Phase I–IV). You will coordinate complex protocols, manage data in OnCore, recruit and consent patients, and ensure regulatory compliance under the CRM.

You will liaise with sponsors, IRB, FDA, and national groups; train staff, optimize workflows, and monitor study performance to advance therapeutic research. Candidates typically have 5–7 years of CRC experience, a BA/BS, and relevant certifications

Qualifications

• 5–7 years of clinical research coordination with BA/BS or equivalent
• Certification by a recognized CRA society (SOCRA/ACRP) desired
• Experience with cancer-related research and regulatory requirements (IRB, FDA)

Responsibilities

• Coordinate Phase I–IV cancer protocols with Good Clinical Practices
• Manage data collection, chart preparation, and record keeping
• Recruit, screen, consent patients and assist PI in visits and questionnaires
• Liaise with sponsors, CROs, and national groups; ensure regulatory compliance

Skills

Interpersonal skills

Communication

Multitasking

Time management

Attention to detail

Problem solving

Team collaboration

Microsoft Office

Education

Bachelor of Arts/Bachelor of Science or equivalent experience

SOCRA/ACRP certification

Tools

OnCore

Microsoft Excel

Job description

UCI Health seeks a Senior Clinical Research Coordinator to support cancer center trials (Phase I–IV). You will coordinate complex protocols, manage data in OnCore, recruit and consent patients, and ensure regulatory compliance under the CRM.

You will liaise with sponsors, IRB, FDA, and national groups; train staff, optimize workflows, and monitor study performance to advance therapeutic research. Candidates typically have 5–7 years of CRC experience, a BA/BS, and relevant certifications