Clinical Research Coordinator

Location: Fully on-site in Gilbert, Arizona, United States

Annual base pay range: $37,800–$94,500

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Coordinate 2–6 clinical trials with varying levels of complexity from study start-up through completion.
• Recruit participants, obtain informed consent, and support participant visits.
• Perform vital signs, phlebotomy, ECGs, and laboratory specimen processing.
• Maintain regulatory documentation and support site audits.
• Work with investigators, sponsors, and clinical monitors on study activities.
• Mentor junior staff and contribute to internal training.

Requirements

• Hands-on experience with vital signs, phlebotomy, ECGs, and laboratory specimen processing.
• Solid understanding of clinical site operations and the drug development process.
• CRC I: 1–3 years of experience at a clinical investigative site working with participants.
• CRC II: At least 3 years of experience as a Clinical Research Coordinator at a clinical investigative site working with participants.
• Strong written and verbal communication, attention to detail, and time-management skills.
• Experience with CTMS, eCRFs, and Microsoft Office.

Culture & Benefits

• Collaborative environment focused on initiative, adaptability, and continuous learning.
• Exposure to multiple therapeutic areas and diverse clinical trials.
• Opportunity to work within a local site management organization backed by a global CRO.
• Health and welfare benefits may be available in addition to the base salary.
• Incentive plans, bonuses, or other compensation may be offered depending on the position.