Senior Clinical Research Coordinator: Integrative Trials

University of California, Irvine; Irvine (CA); On-site; USD 95,000 - 120,000; Full time

Job summary

University of California, Irvine invites applications for a Senior Clinical Research Coordinator to support SSIHI's clinical trials from Phase I to IV. You will coordinate study procedures, manage data, and ensure GCP compliance, SOP adherence, and regulatory requirements across multi-site teams.

In this role, you will recruit and screen participants, obtain consent, maintain trial documentation, and liaise with sponsors, IRB, and NCCIH, contributing to efficient operations and high-quality data

Qualifications

• Bachelor's degree in a related field or equivalent experience.
• Certified Clinical Research Professional (ACRP) preferred.
• Experience coordinating clinical research in healthcare settings.

Responsibilities

• Coordinate all aspects of integrative health trials (Phase I–IV).
• Assist PI with recruitment, screening, consent, and questionnaires.
• Maintain trial documentation and ensure regulatory compliance.

Skills

Public interaction

Record keeping

Multitasking

Data analysis

Independent judgment

Deadline management

Interdisciplinary teamwork

Communication skills

Confidentiality

Attention to detail

Education

Bachelor's degree in related area

ACRP certification

Tools

OnCore

Microsoft Office (Outlook, Word, Excel, PowerPoint)

Job description

University of California, Irvine invites applications for a Senior Clinical Research Coordinator to support SSIHI's clinical trials from Phase I to IV. You will coordinate study procedures, manage data, and ensure GCP compliance, SOP adherence, and regulatory requirements across multi-site teams.

In this role, you will recruit and screen participants, obtain consent, maintain trial documentation, and liaise with sponsors, IRB, and NCCIH, contributing to efficient operations and high-quality data