Pulmonologist -�Clinical Research Investigator

ECN Operating LLC; Tucson (AZ); On-site; USD 150,000 - 200,000; Part time

Job summary

ECN Operating LLC is looking for a committed Physician - Pulmonologist to join our team in Tucson, Arizona. This part-time/per diem position entails serving as a Principal Investigator or Sub-Investigator on clinical trials while ensuring high-quality care for adult patients. Responsibilities include managing chronic conditions, conducting patient assessments, and maintaining compliance with clinical protocols. The ideal candidate must hold an MD or DO degree and possess a valid medical license in Arizona, with board certification in Pulmonology preferred.

Qualifications

• Minimum of 1 year of experience in clinical practice required.
• Current Good Clinical Practice (GCP) certification or willingness to obtain is necessary.
• Prior clinical research experience preferred but not required.

Responsibilities

• Serve as Principal Investigator or Sub‑Investigator on clinical trials.
• Conduct comprehensive physical exams and clinical assessments.
• Evaluate patient eligibility for clinical protocols.
• Provide medical oversight including safety assessments.
• Collaborate with Clinical Research Coordinators and Sponsors.

Skills

Attention to detail

Interpersonal skills

Communication skills

Familiarity with clinical trial protocols

Education

MD or DO degree from an accredited medical school

Valid, unrestricted medical license in Arizona

Board Certified or Board Eligible in Pulmonology

Tools

Electronic medical records (EMRs)

Clinical trial management systems (CTMS)

Job description

Elite Clinical Network (ECN) is seeking a dedicated and research‑oriented Physician – Pulmonologist to join our expanding team of clinical professionals. The ideal candidate will play a critical role in the conduct of clinical trials by serving as a Principal Investigator (PI) or Sub‑Investigator, while continuing to provide high-quality medical care to adult patients within a clinical research setting. This is a part‑time/per diem position with a unique opportunity to contribute to the advancement of medicine through clinical studies.

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 will also be considered.
• Current Good Clinical Practice (GCP) certification or willingness to obtain prior to start.
• Minimum of 1 year of experience in clinical practice; prior clinical research experience preferred but not required.

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 ability to document accurately.
• 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).