Internist - Clinical Research Investigator

ECN Operating LLC; Merrillville (IN); On-site; USD 165,000 - 358,000; Part time

Job summary

ECN Operating LLC is seeking an Internist - Clinical Research Investigator to join our clinical research team on a part-time/per diem basis. The role includes acting as Principal Investigator or Sub-Investigator on multiple Phase I–IV trials and providing medical oversight for trial participants.

The candidate will perform examinations, determine eligibility, ensure protocol compliance, and support recruitment while maintaining regulatory documentation per ICH-GCP and sponsor requirements.

Qualifications

• MD or DO degree required and state medical license.
• Board Certified or Board Eligible in Internal Medicine.
• GCP certification or willingness to obtain before start.
• Minimum 1 year of clinical practice; prior clinical research preferred.

Responsibilities

• Serve as Principal Investigator or Sub-Investigator on Phase I–IV trials.
• Conduct physical exams and eligibility assessments for protocol enrollment.
• Provide medical oversight for trial participants and safety evaluations.
• Ensure document integrity and regulatory compliance (ICH-GCP, FDA).
• Collaborate with sponsors, CRCs, and monitors to support trial operations.

Skills

Clinical research

GCP knowledge

Team collaboration

Communication skills

Education

MD or DO degree

Tools

EMR systems

CTMS

Job description

Career Opportunities with ECN Operating LLC

A great place to work.

Share with friends or Subscribe!

Are you ready for new challenges and new opportunities?

Join our team!

Current job opportunities are posted here as they become available.

Subscribe to our RSS feeds to receive instant updates as new positions become available.

Internist - Clinical Research Investigator

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).