Clinical research Coordinator

Job Description

Job Description

About the Role:

Liver Institute PLLC in Tucson, AZ is looking for a dedicated Clinical Research Coordinator (CRC) to join our specialized team. This is an exciting opportunity to contribute to meaningful clinical research in a focused, patient-centered hepatology practice. If you're passionate about advancing medical science and making a real difference in patients' lives, we want to hear from you!

Qualifications

Bachelor's degree or Higher Required

Minimum of one year of experience as a clinical research coordinator or two years of healthcare experience with patient interaction or related experience

• Excellent interpersonal and relationship-building skills with the ability to communicate effectively with sponsors, research participants, physicians, and clinic staff.
• Strong organizational, time management, and multitasking abilities with exceptional attention to detail.
• Experience with patient recruitment, outreach, or sales/customer engagement is highly preferred.
• Willingness to work a flexible schedule as needed, including occasional early mornings, evenings, or weekends to accommodate participant visits.
• Spanish-speaking (bilingual English/Spanish) preferred.
• Healthcare experience, including phlebotomy skills, is preferred; candidates willing to obtain phlebotomy training will also be considered.
• Educational background in biology, health sciences, nursing, public health, or another life science discipline preferred.
• Strong problem-solving skills with the ability to adapt in a changing environment.
• Demonstrates professionalism, compassion, and a patient-centered approach while maintaining confidentiality and regulatory compliance.

Responsibilities

• Coordinated clinical research studies with multidisciplinary teams.
• Screened, educated, and enrolled study participants.
• Conducted informed consent with participants and caregivers.
• Monitored participant safety and reported adverse events.
• Documented study activities in compliance with regulatory requirements.
• Reviewed and resolved data queries daily.
• Maintained regulatory and study documentation.
• Collected medical history and concomitant medications.
• Requested and reviewed hospital medical records.
• Assisted investigators with clinical trial procedures.
• Processed, prepared, and shipped biological specimens.
• Prepared laboratory requisitions for protocol-required testing.
• Conducted protocol-specific participant interviews and assessments.
• Participated in quality assurance audits.
• Ensured compliance with GCP, protocol, and sponsor requirements.
• Performed additional duties as assigned by the Principal Investigator.

The job is onsite, and no relocation assistance is provided for this position.