Endocrinologist - Clinical Research Investigator

ECN Operating LLC; Scottsdale (AZ); On-site; USD 120,000 - 190,000; Part time

Job summary

ECN Operating LLC is seeking an Endocrinologist to serve as Principal Investigator or Sub-Investigator on multiple Phase I–IV clinical trials in a part-time per diem capacity. The role includes medical oversight, comprehensive exams, and patient management within a clinical research setting.

The ideal candidate will hold an MD/DO with Board Certification in Endocrinology or BE in related fields and a current GCP certification.

Qualifications

• MD or DO degree from an accredited medical school.
• Valid, unrestricted medical license in the state of employment.
• Board Certified or Board Eligible in Endocrinology.
• BC/BE in Family Medicine or Geriatric Medicine will also be considered.
• Current Good Clinical Practice (GCP) certification or willingness to obtain.

Responsibilities

• Serve as Principal Investigator or Sub-Investigator on Phase I–IV trials.
• Perform physical exams and assessments for screening and enrollment.
• Evaluate patient eligibility based on protocol criteria.
• Provide medical oversight including safety assessments and adverse events.
• Collaborate with coordinators, sponsors, and monitors for data integrity.
• Review and sign source documents, CRFs, and regulatory docs.
• Maintain trial documentation compliant with ICH-GCP and FDA.
• Participate in SIVs, Monitoring Visits, and audits as needed.
• Manage chronic and acute conditions per protocol guidelines.
• Educate patients on procedures, consent, and potential side effects.
• Support recruitment and patient retention in trials.

Skills

Clinical Trials

Endocrinology

Patient Care

Regulatory Compliance

Communication Skills

Education

MD/DO degree

BC/BE in Endocrinology

Tools

EMR systems

CTMS

Job description

Career Opportunities with ECN Operating LLC

A great place to work.

Endocrinologist - Clinical Research Investigator

Elite Clinical Network (ECN) 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).