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. 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 #J-18808-Ljbffr