Details:

  • Compensation: $150 - $250/hour
  • Benefits: Medical, Dental, Vision
  • Employment Classification: Direct Hire
  • Status: On-Site
  • Job ID: 21345

Job Title: Physician – Pulmonologist

Work Location: Maricopa County, Arizona

Summary:

This part-time, contract opportunity is ideal for a board-certified pulmonologist interested in clinical research. The role involves serving as a Principal Investigator (PI) or Sub-Investigator for clinical trials, with flexible hours and the potential to integrate research activities into an existing private practice. Compensation is competitive, and the position offers the chance to advance medical knowledge while maintaining patient care responsibilities.

Responsibilities:

  • Act as Principal Investigator or Sub-Investigator for multiple clinical trials across various phases.
  • Conduct physical examinations and clinical assessments to determine participant eligibility for studies.
  • Oversee patient safety, monitor adverse events, and provide ongoing medical care to trial participants.
  • Collaborate with research staff and external partners to ensure adherence to study protocols and regulatory standards.
  • Review and approve clinical documentation, including source documents and case report forms.
  • Maintain accurate and compliant records in accordance with regulatory and sponsor requirements.
  • Participate in site visits, monitoring activities, and audits as required by study protocols.
  • Support patient recruitment, retention, and education regarding study procedures and informed consent.

Qualifications:

  • MD or DO degree from an accredited institution.
  • Active, unrestricted medical license in Arizona.
  • Board Certification or Board Eligibility in Pulmonology; Family Medicine or Geriatric Medicine also considered.
  • Current or willingness to obtain Good Clinical Practice (GCP) certification.
  • Minimum of 1 year of clinical practice experience; clinical research experience preferred but not required.
  • Familiarity with FDA, ICH-GCP, and clinical trial protocols is advantageous.
  • Strong documentation, communication, and teamwork skills.
  • DEA license preferred; experience with EMRs and CTMS is a plus.

Published Category: Clinical Research

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