Physician - Pulmonologist

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.

• 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.

• 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.

• 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).

Mid‑Senior level

Part‑time

Strategy/Planning and Information Technology