Clinical Research Coordinator II/III — Impactful Trials

Arizona Liver Health; Chandler (AZ); On-site; USD 38,000 - 50,000; Full time

Benefits offered by this job

Health, Dental, Vision

3 weeks PTO

401K with 6% company match

Disability

CEUs / Educational Assistance

Job summary

Arizona Liver Health in Chandler is seeking a Clinical Research Coordinator II or III (CRC 2-3) to oversee clinical research activities under the PI or sub-investigator. The role focuses on protocol coordination, data management, and patient recruitment, in a fast-paced clinical trials environment.

The position requires at least 2 years of CRC experience in late-phase trials, GCP knowledge, and strong regulatory compliance capabilities.

Qualifications

• Minimum 2 years of experience as a Clinical Research Coordinator for late-phase trials.
• Experience and training in clinical research, including IRB submissions and trial enrollment management.
• Thorough understanding of regulatory requirements, GCP, and biomedical research ethics.
• Interpersonal and communication skills to work with staff, sponsor, and participants.

Responsibilities

• Manage conduct of clinical research activities under the PI or sub-investigator.
• Coordinate and implement assigned protocols in compliance with FDA CFR, GCP and SOPs.
• Recruit and screen potential participants and manage follow-ups with referrals.
• Maintain study files, data entry, and source documentation.
• Monitor and report adverse events and ensure regulatory compliance.

Skills

Clinical Research

GCP Knowledge

Communication Skills

Education

Associates or Bachelor's degree

Tools

Data management software

Job description

Arizona Liver Health in Chandler is seeking a Clinical Research Coordinator II or III (CRC 2-3) to oversee clinical research activities under the PI or sub-investigator. The role focuses on protocol coordination, data management, and patient recruitment, in a fast-paced clinical trials environment.

The position requires at least 2 years of CRC experience in late-phase trials, GCP knowledge, and strong regulatory compliance capabilities.