What are the responsibilities and job description for the Clinical Research Pulmonologist position at Protouch Staffing?
Location: Glendale, AZ (85304)
Employment Type: 1099 | Part-Time (0-8 hours/ week)
Position Overview
Seeking a research-oriented Pulmonologist to join our clinical research team in Sun City, AZ. This role offers a unique opportunity to serve as a Principal Investigator (PI) or Sub-Investigator on Phase I-IV clinical trials while providing high-quality medical care to adult patients in a clinical research setting.
Key Responsibilities
Employment Type: 1099 | Part-Time (0-8 hours/ week)
Position Overview
Seeking a research-oriented Pulmonologist to join our clinical research team in Sun City, AZ. This role offers a unique opportunity to serve as a Principal Investigator (PI) or Sub-Investigator on Phase I-IV clinical trials while providing high-quality medical care to adult patients in a clinical research setting.
Key Responsibilities
- Serve as Principal Investigator or Sub-Investigator on Phase I-IV clinical trials
- Conduct physical exams, clinical assessments, and protocol screenings
- Determine patient eligibility based on study inclusion/exclusion criteria
- Provide medical oversight, safety monitoring, and adverse event evaluations
- Collaborate with Clinical Research Coordinators, Sponsors, and Monitors
- Review and sign source documents, CRFs, and regulatory documentation
- Ensure compliance with ICH-GCP, FDA, and sponsor requirements
- Participate in Site Initiation Visits (SIVs), monitoring visits, and audits
- Manage chronic and acute conditions per protocol and standard of care
- Educate patients on informed consent, study procedures, and potential risks
- Support patient recruitment and retention efforts
- MD or DO from an accredited medical school
- Active, unrestricted Arizona medical license
- Board Certified or Board Eligible in Pulmonology
- BC/BE in Family Medicine or Geriatrics will also be considered
- Minimum 1 year of clinical experience
- GCP certification (or willingness to obtain prior to start)
- Clinical research or industry-sponsored trial experience
- Knowledge of FDA regulations and ICH-GCP guidelines
- Strong documentation and attention to detail
- Excellent communication and interpersonal skills
- Experience with EMRs and CTMS platforms
- DEA license preferred
Salary : $100 - $200