Endocrinologist - Clinical Research Investigator

ECN Clinical; Denver (CO); On-site; USD 124,000 - 207,000; Part time

Job summary

ECN Clinical is seeking an Endocrinologist for a part-time per diem role as a Clinical Research Investigator. You will serve as a Principal Investigator or Sub-Investigator on Phase I–IV trials, oversee patient evaluations, and ensure protocol compliance in a clinical research setting.

The role emphasizes medical oversight, informed consent, safety monitoring, and collaboration with sponsors and study teams. Prior GCP experience is preferred and licensure is required.

Qualifications

• MD or DO degree
• Unrestricted medical license in the state of employment
• Board Certified or Board Eligible in Endocrinology
• BC/BE in Family Medicine or Geriatric Medicine also considered
• Current Good Clinical Practice (GCP) certification or willing to obtain before start
• Minimum 1 year of clinical practice; clinical research exp preferred but not required

Responsibilities

• Serve as Principal Investigator or Sub-Investigator on multiple Phase I–IV trials.
• Perform comprehensive physical exams and protocol screening/enrollment assessments.
• Evaluate patient eligibility based on inclusion/exclusion criteria.
• Provide medical oversight and safety assessments for trial participants.
• Collaborate with CR Coordinators, Sponsors, and Monitors for protocol compliance and data integrity.
• Review and sign source documents, CRFs, and regulatory paperwork.

Skills

Attention to detail

Communication skills

Team collaboration

EMR/CTMS experience

Clinical research acuity

Education

MD or DO degree

Unrestricted medical license (state)

Board Certified/Eligible in Endocrinology

BC/BE in Family Medicine or Geriatric Medicine considered

GCP certification

1 year clinical practice

Job description

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Endocrinologist - Clinical Research Investigator

ECN Clinical is seeking a dedicated and research-oriented Endocrinologist - 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 Endocrinology.
• 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).