Hepatology Research APP — Clinical Trials

Arizona Liver Health

Tucson (AZ)

On-site

USD 110,000 - 150,000

Full time

14 days+
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Benefits offered by this job

Health benefits
PTO 4 weeks
CME budget
Sick time
Holidays
401K match
Disability
Company vehicle

Job summary

Arizona Liver Health in Tucson, AZ is seeking an experienced Research Advanced Practice Provider (NP/PA) to support hepatology clinical trials on site. You will evaluate patients, review pretreatment criteria, and guide participants through liver disease studies.

The role requires prior clinical research experience, GI/hepatology knowledge, and proficiency with EMR systems. You will educate patients about trial options, coordinate visits with study teams, and ensure compliant documentation from

Qualifications

  • Licensed NP or PA with clinical research experience.
  • Experience in gastroenterology/hepatology and research protocols.
  • Proficient in EMR systems and Microsoft Office.

Responsibilities

  • Perform patient evaluations and pretreatment reviews for standard of care and research patients.
  • Educate patients on therapeutic options through available liver trials onsite.
  • Oversee patient care in clinical trials and safety reviews.
  • Coordinate with clinical research staff to complete visits and document properly.
  • Take study and patient from first visit to closeout.

Skills

Clinical research experience
Nurse Practitioner or PA license
GI/hepatology knowledge
EMR (eCW)
Communication skills
Spanish preferred

Education

Bachelor's Degree in Nursing and NP/PA program

Tools

eCW EMR
MS Office

Job description

Arizona Liver Health in Tucson, AZ is seeking an experienced Research Advanced Practice Provider (NP/PA) to support hepatology clinical trials on site. You will evaluate patients, review pretreatment criteria, and guide participants through liver disease studies.

The role requires prior clinical research experience, GI/hepatology knowledge, and proficiency with EMR systems. You will educate patients about trial options, coordinate visits with study teams, and ensure compliant documentation from

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