A Clinical Investigator works on a clinical trial, and is responsible for ensuring that an investigation is conducted according to the signed investigator statement, the investigational plan, and applicable regulations; for protecting the rights, safety, and welfare of subjects under the investigator's care; and for the control of drugs under investigation. The Clinical Investigator must also meet requirements set forth by the FDA, EMA or other regulatory body. The qualifications must be outlined in a current resume and readily available for auditors.
Part-Time (0-8 hours) They do not need to have to work or own their own private practice, but it is preferred. It is preferred due to it being easier for the PI to potentially do any procedures at their clinic or refer patients to our trials for additional compensation. About the Role We are seeking a board-certified to serve as a Clinical Research Pulmonologist You will oversee protocol compliance, ensure patient safety, and collaborate with sponsors, CROs, and cross-functional teams to drive the success of Phase I-IV clinical trials. Key Responsibilities Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for dermPulmonologist atology-focused and multi-therapeutic clinical trials. Conduct medical screenings, Pulmonologist assessments, and physical examinations for study participants. Provide clinical oversight and medical care to study subjects in accordance with protocols, ICH-GCP, and regulatory requirements. Collaborate with study coordinators, nurses, and research staff to ensure compliance and accurate documentation. Document all patient interactions, adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems . Establish and maintain strong working relationships with sponsors, CROs, monitors, and IRBs. Participate in site initiation visits (SIVs), monitoring visits, and audits . Contribute to protocol feasibility reviews, study design input, and recruitment strategies . Attend investigator meetings and provide medical expertise on dermatology-related endpoints and safety monitoring. Stay current on clinical research regulations and advances in Pulmonologist and investigational therapies . Qualifications M.D. or D.O. with an active, unrestricted Arizona medical license . Board certification in Pulmonologist required. Valid DEA license and
BLS/ACLS
certification . Prior experience in clinical research/clinical trials strongly preferred (training available for motivated candidates). Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS) . Strong interpersonal and communication skills with the ability to work in a multidisciplinary, fast-paced environment . Commitment to ethical research practices and patient-centered care. Compensation & Benefits Competitive hourly rate: up to $250 per hour based on experience. Flexible part-time schedule. Opportunity to participate in groundbreaking research and expand expertise in Pulmonologist and clinical trials. #INDPRO
