Pulmonologist - Clinical Research Investigator

ECN Clinical

Tucson (AZ)

In loco

USD 180.000 - 240.000

Part-time

7 giorni fa
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Descrizione del lavoro

ECN Clinical is seeking a Pulmonologist - Clinical Research Investigator to join our team as a Principal Investigator or Sub-Investigator in a part-time per diem role. The position focuses on conducting clinical trials and providing high-quality medical care to adult patients within a research setting.

Responsibilities include overseeing trials, protocol compliance, safety assessments, and collaboration with sponsors and coordinators.

Competenze

  • 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.
  • GCP certification or willingness to obtain prior to start.
  • Minimum of 1 year of clinical practice; prior clinical research experience preferred but not required.

Mansioni

  • Serve as Principal Investigator or Sub-Investigator on multiple Phase I–IV clinical trials.
  • Perform comprehensive physical exams and assessments for protocol screening and enrollment.
  • Evaluate patient eligibility based on inclusion/exclusion criteria of clinical protocols.
  • Provide medical oversight for trial participants, including safety assessments and ongoing care.
  • Collaborate with Coordinators, Sponsors, and Monitors to ensure protocol compliance and data integrity.
  • Review and sign off on source documents, CRFs, and regulatory documentation.
  • Maintain detailed clinical trial documentation in compliance with ICH-GCP, FDA, and sponsor requirements.
  • Participate in Site Initiation Visits, Monitoring Visits, and Audits as needed.
  • Manage chronic and acute conditions among study participants per protocol guidelines.
  • Educate and counsel patients on study procedures and informed consent.
  • Support recruitment efforts and promote patient retention in trials.

Conoscenze

Medical license
GCP certification
Pulmonology BC/BE
Clinical research experience
Regulatory documentation

Formazione

MD or DO degree

Strumenti

EMR/CTMS familiarity

Descrizione del lavoro

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Pulmonologist -Clinical Research Investigator

ECN Clinical is seeking a dedicated and research-oriented Pulmonologist - Clinical Research Investigator to join our expanding team of clinical professionals. The ideal candidate will play a critical role in the conduct of clinical trials by serving as a Principal Investigator (PI) or Sub-Investigator, while continuing to provide high-quality medical care to adult patients within a clinical research setting. This is a part time/per diem position with a unique opportunity to contribute to the advancement of medicine through clinical studies.

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 will also be considered.
  • Current Good Clinical Practice (GCP) certification or willingness to obtain prior to start.
  • Minimum of 1 year of experience in clinical practice; prior clinical research experience preferred but not required.

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 ability to document accurately.
  • 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).
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