Internist - Clinical Research Investigator

Elite Clinical Network; Merrillville (IN); On-site; USD 90,000 - 150,000; Part time

Job summary

Elite Clinical Network (ECN) is seeking an Internist - Clinical Research Investigator to join our Clinical Research team as PI or Sub-Investigator in a part-time, per-diem role. The physician will oversee trials and provide patient care within a research setting.

The successful candidate will conduct physical exams, evaluate eligibility, ensure protocol compliance, and collaborate with sponsors and monitors to maintain data integrity and participant safety.

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 Internal Medicine.
• GCP certification or willingness to obtain prior to start.

Responsibilities

• Serve as Principal Investigator or Sub-Investigator on multiple Phase I–IV clinical trials.
• Perform comprehensive physical exams and protocol screenings for enrollment.
• Evaluate patient eligibility based on inclusion/exclusion criteria of protocols.
• Provide medical oversight for trial participants, including safety assessments and AE evaluations.
• Collaborate with CR Coordinators, Sponsors, and Monitors to ensure protocol compliance and data integrity.
• Review and sign source documents, CRFs, and regulatory documentation.
• Maintain detailed clinical trial documentation per 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 as per protocol guidelines.
• Educate and counsel patients on study procedures, informed consent, and potential side effects.

Skills

Internal Medicine

Clinical Research

Patient care

Team collaboration

Education

MD/DO

Tools

EMR Systems

CTMS

CRF review

Job description

Position Overview

Elite Clinical Network (ECN) is seeking a dedicated and research-oriented Internist - 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 Internal Medicine.


• 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).