Clinical Research Coordinator
US$28 – US$36 / hr base salary
Posted 29 Sep 2026
Advertised as “Clinical Research Coordinator II/III”
BranchFactor Summary
The original posting with the fluff stripped out
- Level
- II/III
- Expected experience
- 2+ yrs
- Management level
- People management
- Employment
- On-Site
- Contract
- Full-time
| Base salary | US$28 – US$36 / hr |
|---|
CertificationsGCP Certification
Field of studyClinical Research Management, Healthcare (or related)
Study levelAssociate degree or higher
Study levelMaster's
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 Clinical Trials is looking for qualified candidates for the Clinical Research Coordinator II / III position in Chandler
Title: Clinical Research Coordinator II or III
Compensation: $27.50 to $36.06 per hour depending on experience and qualifications
Status: Full-time
Location: Chandler, AZ (Onsite)
Schedule: 7am - 4pm (Monday-Friday)
Essential job functions/duties:
Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.
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Under the direction of the Principal Investigator or sub-investigator, manage the conduct of clinical research activities.
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Responsible for coordinating and implementing assigned protocols in compliance with FDA CFR, GCP and company SOPs.
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Collects and records clinical research data, assists in patient assessments, scheduling, maintain study files, study supplies and study medication accountability.
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Develop management systems and prepare for study initiation
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Review with the Principal Investigator the inclusion/exclusion criteria, overall structure and requirements of each protocol
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Review the protocol summary sheet and the Informed Consent Form for accuracy and clarity about these protocols to staff and patients.
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Responsible for the recruitment and screening of potential participants, which includes chart review of patients and schedules, contacting leads from outside recruitment efforts, and following up on referrals from all sources.
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Responsible for meeting recruitment goals for each study.
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May assume primary responsibility in the implementation and management of new clinical trials in a knowledgeable and collaborative manner.