Gastroenterologist - Clinical Research Investigator

Elite Clinical Network; Long Beach (CA); On-site; USD 150,000 - 250,000; Part time

Job summary

A clinical research organization seeks a dedicated Physician – Gastroenterologist, offering a part-time opportunity to engage in clinical trials as a Principal Investigator. Candidates must hold an MD or DO degree and have a valid medical license in California. Responsibilities include evaluating patient eligibility, providing medical oversight, and ensuring compliance with clinical protocols. Ideal for those interested in contributing to medical advancements while maintaining quality patient care.

Qualifications

• Must possess a valid medical license in California.
• Experience in clinical practice with a preference for clinical research.
• Strong background in gastroenterology preferred.

Responsibilities

• Serve as Principal Investigator on multiple clinical trials.
• Evaluate patient eligibility for clinical protocols.
• Provide medical oversight for trial participants.
• Collaborate with research teams to ensure compliance.

Skills

Patient interaction

Documentation accuracy

Interpersonal communication

Collaboration in research

Education

MD or DO degree from an accredited medical school

Valid, unrestricted medical license

BC/BE in Gastroenterology

Current Good Clinical Practice (GCP) certification

Minimum of 1 year of clinical practice

Job description

Physician - Gastroenterologist

Join to apply for the Physician - Gastroenterologist role at Elite Clinical Network.

Position Overview

Elite Clinical Network (ECN) is seeking a dedicated and research-oriented Physician – Gastroenterologist 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 Gastroenterology.
• 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).

Seniority Level

Mid-Senior level

Employment Type

Part-time

Job Function

Strategy/Planning and Information Technology