Clinical Research Coordinator II (CRC2) Flagstaff

About this role

About Us:

Arizona Liver Health (ALH) is dedicated to driving high standards of care and advancing medical innovation through leading clinical trials, ensuring patient safety and regulatory compliance, and generating high-quality clinical data. Our network of multiphase, multitherapeutic research, standard of care, and VEN Centers sites is staffed by skilled providers, research, clinic, pharmacy, and patient outreach professionals. ALH operates state-of-the-art facilities and programs to meet the evolving needs of clinical research and overall patient treatment.

Job Summary:

Arizona Liver Health/Arizona Clinical Trials is looking for qualified candidates for the Clinical Research Coordinator II position in Flagstaff.

Title: Clinical Research Coordinator II (CRC2)

Compensation: $27.50 - $36.00 per hour, depending on experience and qualifications

Status: Full-time, Non-exempt, Hourly

Location: Flagstaff, AZ (onsite) Monday-Friday, 7am-4pm

Essential job functions/duties:

Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.

Participant Recruitment & Enrollment:

• Identify, screen, and recruit eligible participants according to study protocol and inclusion/exclusion criteria.

• Conduct informed consent process and ensure documentation is complete and properly stored.

• Maintain participant retention efforts; schedule and follow up with participants for visits and assessments.

Research Procedures & Clinical Duties:

• Phlebotomy: collect, label, process, and ship blood and other biospecimens as required.

• Pharmacy Tech: assist with investigational drug handling, storage, dispensing, accountability logs, and inventory management of study medications or investigational products as permitted.

• Take vital signs, height/weight measurements, ECGs (if applicable), and other protocol‐specified assessments

• Follow study procedures to ensure participant safety, monitor adverse events (AEs) and serious adverse events (SAEs), report as required.

Data Management & Entry:

• Enter data accurately into source documents and electronic databases / Electronic Data Capture (EDC) systems.