Hepatology Clinical Research Coordinator

Liver Institute PLLC; Tucson (AZ); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Employee discounts

Job summary

Liver Institute PLLC in Tucson, AZ seeks a dedicated Clinical Research Coordinator to support hepatology studies within a patient-centered, multidisciplinary team. You will screen participants, educate them about studies, obtain informed consent, coordinate study visits, and ensure safety reporting and accurate data capture.

Qualifications include a Bachelor's degree or higher and at least one year of CRC experience or two years healthcare with patient interaction.

Qualifications

• Bachelor's degree or higher required.
• Minimum of one year of CRC experience or two years of healthcare experience with patient interaction.
• Excellent interpersonal and relationship-building skills with sponsors, participants, physicians and staff.
• Strong organizational and multitasking abilities with attention to detail.
• Experience with participant recruitment/outreach or patient engagement preferred.
• Willingness to work a flexible schedule including mornings, evenings or weekends.
• Spanish-speaking (bilingual) preferred; phlebotomy training considered.
• Background in biology/health sciences preferred; focus on confidentiality and compliance.

Responsibilities

• Coordinate clinical research studies with multidisciplinary teams.
• Screen, educate, and enroll study participants.
• Obtain informed consent from participants and caregivers.
• Monitor participant safety and report adverse events.
• Document study activities per regulatory requirements.
• Review and resolve data queries daily.

Skills

Communication

Organization

Time management

Attention to detail

Participant recruitment

Flexibility

Spanish bilingual (preferred)

Regulatory compliance

Problem-solving

Education

Bachelor's degree or higher

Job description

Liver Institute PLLC in Tucson, AZ seeks a dedicated Clinical Research Coordinator to support hepatology studies within a patient-centered, multidisciplinary team. You will screen participants, educate them about studies, obtain informed consent, coordinate study visits, and ensure safety reporting and accurate data capture.

Qualifications include a Bachelor's degree or higher and at least one year of CRC experience or two years healthcare with patient interaction.