Clinical Research Coordinator

Clinical Research Coordinator II/III

We are seeking a motivated Clinical Research Coordinator (CRC) II/III to support and manage clinical trials focused on liver health and related conditions. This role is responsible for coordinating patient visits, executing study protocols, and ensuring compliance with regulatory guidelines.

The ideal candidate is detail-oriented, patient-focused, and comfortable working in a fast-paced research environment. Due to our diverse patient population, bilingual English/Spanish candidates are strongly preferred.

Location: Peoria, AZ

Schedule: Full-time

Key Responsibilities

• Coordinate and execute clinical trial activities in accordance with study protocols, GCP, and regulatory requirements
• Conduct patient visits, including screening, enrollment, and follow-up assessments
• Obtain informed consent from study participants (including high-volume/mass consenting when applicable)
• Collect, process, and ship laboratory specimens (phlebotomy can be trained on-site)
• Accurately enter and maintain study data in CTMS and other systems
• Maintain source documentation and regulatory binders
• Communicate with study sponsors, CROs, and internal stakeholders
• Monitor patient safety and report adverse events per protocol guidelines
• Support multiple clinical trials simultaneously based on level

Leveling Overview

Clinical Research Coordinator II

• Manages 23 clinical trials concurrently
• Supports study operations with moderate oversight
• Assists with sponsor communication

Clinical Research Coordinator III

• Manages 3+ clinical trials independently
• Leads study coordination efforts across multiple protocols
• Serves as primary point of contact for sponsors and CROs
• Mentors junior coordinators as needed

Required Qualifications

• Experience supporting sponsor-initiated or interventional clinical trials
• Hands-on experience with: patient consenting, data entry and CTMS systems, laboratory processing
• Strong organizational and communication skills
• Ability to manage multiple priorities and patient visits efficiently

Education & Experience (one of the following):

• Bachelor's degree + relevant clinical research experience (required for Level II)
• Foreign medical degree + 1+ year of clinical research experience
• High school diploma + 45 years of clinical research experience

Preferred Qualifications

• Bilingual in English and Spanish (highly preferred due to patient population; ~25% Spanish-speaking)
• Phlebotomy experience (or willingness to learn)
• Experience working in high-volume patient settings
• Familiarity with relatively low-complexity trials (e.g., vaccine/flu studies)

Employee Value Proposition (EVP)

• Collaborative and mission-driven clinical research environment
• Opportunity to gain exposure to a variety of clinical trials, including interventional studies
• Strong team support with stable recruitment pipelines
• Ability to make a direct impact on patient care and clinical advancements

Job Type & Location: This is a Contract position based out of Chandler, AZ.

Pay and Benefits: The pay range for this position is $27.00 - $36.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type: This is a fully onsite position in Chandler, AZ.

Application Deadline: This position is anticipated to close on Jun 18, 2026.