Clinical Research Coordinator II — Lead Multiphase Trials

Arizona Liver Health; Tucson (AZ); On-site; USD 39,000 - 45,000; Full time

Benefits offered by this job

Health, Dental, Vision

Paid time off

401(k) match

Educational assistance

Job summary

Arizona Liver Health/Arizona Clinical Trials is seeking a qualified Clinical Research Coordinator II in Tucson, AZ. The role focuses on coordinating and managing clinical studies, with duties spanning data collection, patient screening, and regulatory compliance.

The CRC2 will work under the PI and cross‑functionally with team members to ensure protocol adherence and quality data, while supporting patient safety and trial integrity in a fast‑paced environment.

Qualifications

• Minimum 2 years as a Clinical Research Coordinator for late‑phase trials.
• Experience with regulatory requirements and GCP; IRB submissions and source documentation.
• Strong interpersonal and communication skills for sponsors, staff and patients.

Responsibilities

• Manage conduct of clinical research activities under PI or sub‑investigator.
• Coordinate and implement protocols in compliance with FDA CFR, GCP and SOPs.
• Recruit and screen participants, maintain study files, and track visits and stipends.
• Ensure data accuracy, perform data entry, review protocols and source documentation.
• Support audits, regulatory inspections, and training of staff.

Skills

Clinical Research Coordinator

Regulatory compliance

Data collection

Communication skills

Education

Associates or Bachelor's degree in healthcare/clinical research

Tools

EDC systems

IRB submission software

Study management software

Job description

Arizona Liver Health/Arizona Clinical Trials is seeking a qualified Clinical Research Coordinator II in Tucson, AZ. The role focuses on coordinating and managing clinical studies, with duties spanning data collection, patient screening, and regulatory compliance.

The CRC2 will work under the PI and cross‑functionally with team members to ensure protocol adherence and quality data, while supporting patient safety and trial integrity in a fast‑paced environment.