Pulmonologist - Clinical Research Investigator

Elite Clinical Network; Tucson (AZ); On-site; USD 100,000 - 200,000; Part time

Job summary

A leading clinical network is seeking a dedicated Physician – Pulmonologist for a part-time position. In this role, you will act as Principal Investigator or Sub-Investigator in clinical trials while ensuring top-notch patient care. The ideal candidate will have an MD or DO degree, relevant clinical experience, and a valid medical license in Arizona. You will collaborate closely with research teams and maintain compliance with clinical protocols. Join us to contribute to medical advancements in a supportive environment.

Qualifications

• ED or DO degree from an accredited medical school.
• Unrestricted medical license in Arizona.
• Minimum of 1 year of clinical practice experience.

Responsibilities

• Serve as Principal Investigator on clinical trials.
• Perform physical exams and clinical assessments.
• Review and sign off on clinical trial documentation.

Skills

Attention to detail

Communication skills

Team collaboration

Education

MD or DO degree

Valid medical license

Board Certified or Board Eligible in Pulmonology

Tools

Electronic medical records (EMRs)

Clinical trial management systems (CTMS)

Job description

Physician – Pulmonologist (Part‑Time/Per Diem)

Position Overview: Elite Clinical Network (ECN) seeks a dedicated and research‑oriented Physician – Pulmonologist to serve as Principal Investigator or Sub‑Investigator in clinical trials while providing adult patient care within a research setting. This part‑time/per diem role offers a unique opportunity to contribute to medical advancement.

Key Responsibilities

• Serve as Principal Investigator or Sub‑Investigator on multiple Phase I–IV clinical trials.
• Perform comprehensive physical exams and clinical assessments for protocol screening and enrollment.
• Evaluate patient eligibility based on inclusion/exclusion criteria of clinical protocols.
• Provide medical oversight for clinical trial participants, including safety assessments, adverse event evaluations, and ongoing care.
• Collaborate closely with Clinical Research Coordinators, Sponsors, and Monitors to ensure protocol compliance and data integrity.
• Review and sign off on source documents, case report forms (CRFs), and regulatory documentation.
• Maintain detailed and accurate clinical trial documentation in compliance with ICH‑GCP, FDA, and sponsor requirements.
• Participate in Site Initiation Visits (SIVs), Monitoring Visits, and Audits as needed.
• Manage chronic and acute conditions among study participants in alignment with standard care and protocol guidelines.
• Educate and counsel patients on study procedures, informed consent, and potential side effects.
• Support recruitment efforts and promote patient retention in trials.

Qualifications

• MD or DO degree from an accredited medical school.
• Valid, unrestricted medical license in the state of employment.
• Board Certified or Board Eligible (BC/BE) in Pulmonology.
• BC/BE in Family Medicine or Geriatric Medicine considered.
• Current Good Clinical Practice (GCP) certification or willingness to obtain prior to start.
• Minimum of 1 year of clinical practice experience; prior clinical research experience preferred.

Preferred Skills

• Familiarity with FDA, ICH‑GCP, and clinical trial protocols.
• Experience managing or participating in industry‑sponsored clinical trials.
• Strong attention to detail and accurate documentation.
• Excellent interpersonal and communication skills for patient interaction and sponsor collaboration.
• Ability to work collaboratively with a cross‑functional team in a fast‑paced research environment.
• Comfortable using electronic medical records (EMRs) and clinical trial management systems (CTMS).
• DEA license (preferred).

Seniority Level

Mid‑Senior level

Employment Type

Part‑time

Job Function

Strategy/Planning and Information Technology