What are the responsibilities and job description for the Clinical research Coordinator position at Liver Institute PLLC?
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.
Salary : $17 - $20