Physician - Radiologist

Elite Clinical Network; Houston (TX); On-site; USD 150,000 - 200,000; Part time

Job summary

A leading clinical research organization seeks a dedicated Physician – Radiologist/Interventional Radiologist, Gastroenterologist, or Hepatologist in Houston, Texas. The role involves serving as a Principal Investigator or Sub-Investigator on clinical trials while providing quality medical care. The ideal candidate must have an MD or DO, relevant certifications, and at least one year of experience in clinical practice. This part-time position offers a unique opportunity to contribute to advancements in medicine through clinical research.

Qualifications

• Must have liver biopsy capability at practice location.
• MD or DO degree from an accredited medical school.
• Valid, unrestricted medical license in the state of employment.
• Board Certified or Board Eligible in Radiology or Gastroenterology.
• Minimum of 1 year of clinical practice experience required.

Responsibilities

• Serve as Principal Investigator or Sub‑Investigator on clinical trials.
• Evaluate patient eligibility based on inclusion/exclusion criteria.
• Provide medical oversight for clinical trial participants.
• Collaborate with Clinical Research Coordinators and Sponsors.
• Maintain accurate clinical trial documentation.

Skills

Liver biopsy capability

Interpersonal and communication skills

Attention to detail

Ability to work collaboratively

Education

MD or DO degree

Board Certified or Board Eligible in Radiology, Gastroenterology, and Hepatology

Tools

Electronic medical records (EMRs)

Clinical trial management systems (CTMS)

GCP certification

Job description

Position Overview

Elite Clinical Network (ECN) is seeking a dedicated and research-oriented Physician – Radiologist/Interventional Radiologist, Gastroenterologist, or Hepatologist 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.

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

• Must have liver biopsy capability at practice location.
• 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 Radiology, Gastroenterology, and Hepatology.
• 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).
• DEA license (preferred).