Internist - Clinical Research Investigator

Elite Clinical Network; Carrollton (TX); On-site; USD 138,000 - 207,000; Part time

Job summary

A healthcare organization in Texas is seeking a Physician – Internist to join their team. This part-time role involves serving as a Principal Investigator or Sub-Investigator on clinical trials, evaluating patient eligibility, and providing medical oversight. The ideal candidate will have an MD or DO degree and a valid medical license in Texas, along with at least 1 year of clinical practice experience. This position offers the chance to contribute to clinical research while delivering high-quality medical care.

Qualifications

• Minimum of 1 year of experience in clinical practice.
• Willingness to obtain current Good Clinical Practice (GCP) certification.
• Prior clinical research experience preferred.

Responsibilities

• Serve as Principal Investigator or Sub-Investigator on clinical trials.
• Perform comprehensive physical exams for patient screening.
• Evaluate patient eligibility based on clinical protocols.
• Maintain clinical trial documentation in compliance with regulations.

Skills

Familiarity with FDA regulations

Strong attention to detail

Excellent interpersonal skills

Ability to work collaboratively

Communication

Education

MD or DO degree from an accredited medical school

Valid medical license in Texas

Board Certified or Board Eligible in Internist

Tools

EMR

CTMS

Job description

Position Overview

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