Research Physician - Principal Investigator (Tucson)

Arizona Liver Health • Tucson, AZ

7d • Onsite

About The Position

Arizona Liver Health (ALH) is dedicated to driving high standards of care and advancing medical innovation through leading clinical trials, ensuring patient safety and regulatory compliance, and generating high-quality clinical data. Our network of multiphase, multitherapeutic research, standard of care, and VEN Centers sites is staffed by skilled providers, research, clinic, pharmacy, and patient outreach professionals. ALH operates state-of-the-art facilities and programs to meet the evolving needs of clinical research and overall patient treatment.
As a Clinical Research Physician (PI), you will serve the Principal Investigator on various clinical trials/studies to oversee the treatment and management of multi-organ diseases and conditions. This position will be responsible for the clinical oversight/care of research patients and the recruitment, screening, and randomization of patient subjects while ensuring regulatory compliance and data accuracy.

Requirements

• Extensive clinical experience in diagnosing and managing diseases that involve multiple organ systems.
• Mastery in interpreting complex diagnostic tests and using them for integrated treatment planning.
• Strong interpersonal and communication skills for patient interaction and collaboration with internal medical teams.
• Ability to interpret complex data and make data-driven decisions to contribute to the advancement of medical knowledge.
• Medical degree (MD, DO, or equivalent) from an accredited institution required
• Board certification in relevant specialty (ie. Internal Medicine, Family Medicine, Gastroenterology, Hepatology) required
• Active medical license with ability to practice in Arizona without restrictions required
• Able to lift at least 25 lbs.
• Able to stand for long periods (at least 80%)
• Able to type and do computer work for long periods
• Must have valid documentation and authorization to work in the U.S.

Nice To Haves

• Proven experience in conducting clinical research and serving as a Primary Investigator for clinical trials is highly preferred.
• Strong understanding of clinical trial methodologies, regulatory guidelines, as well as Good Clinical Practice (GCP) strongly preferred.
• Leadership and mentorship experience within a healthcare setting is preferred.
• Experience in academic medicine or clinical research related to multi-organ diseases preferred.
• Knowledge of statistical analysis and data management for clinical trials is highly preferred.
• Additional fellowship training preferred

Responsibilities

• Serve as the Principal Investigator (PI) for clinical trials related to the treatment and management of multi-organ diseases.
• Clinical decision making & management of patients in trials.
• Ensure clinical trials comply with regulatory requirements, ethical standards, and institutional protocols.
• Recruit, screen, and enroll eligible patients for various clinical studies, ensuring informed consent and patient safety throughout the trial process.
• Supervise and train clinical research APPs
• Oversee the collection and analysis of clinical data, ensuring accuracy and integrity in study results.
• Coordinate with research teams, sponsors, and regulatory agencies to ensure the smooth operation and completion of clinical trials.
• Review clinical trial outcomes and provide detailed reports and recommendations based on findings.
• Subject Matter Expert on insights for business development (BD) for future trial pipeline.
• Ensure the protection of patient rights and confidentiality throughout the research process.
• Mentor and supervise junior researchers, clinicians, and research staff involved in clinical trials.
• Contribute to the writing of clinical trial publications, presenting findings at scientific conferences, and collaborating with academic institutions on research initiatives.
• Execute required trainings as assigned by the Regulatory and Compliance department in the timely manner.
• Participate in sponsor monitor visits and ensure questions are answered in a timely manner.
• Work with BD team to maintain sponsor/CRO relationships and develop trial pipeline.

Benefits

• Health, Dental, Vision (with HSA plans and employer contribution) begins 1st of the month after hire
• 6 weeks of PTO
• Continuing Medical Education budget (CME) and necessary time off
• 5 Days Sick Time
• 7 Company Holidays + 2 Half-Days
• 401K with company 6% match (quarterly enrollment, company matches biweekly aligned to payroll periods)
• Short & Long Term Disability
• Shared company vehicles for required travel

What This Job Offers

• Job Type: Full-time
• Career Level: Principal
• Education Level: Ph.D. or professional degree