Endocrinologist - Clinical Research Investigator

ECN Clinical; Scottsdale (AZ); On-site; USD 129,000 - 203,000; Part time

Benefits offered by this job

Flexible per diem schedule

Professional development

Job summary

ECN Clinical is seeking an Endocrinologist to join as a Clinical Research Investigator, serving as Principal Investigator or Sub-Investigator. The role is part-time/per diem and focuses on conducting phase I–IV trials while continuing to provide adult medical care in a clinical research setting.

The ideal candidate holds an MD/DO, is licensed, and boarded in Endocrinology (or related fields with BC/BE). GCP certification or willingness to obtain is required; experience in clinical practice and

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.

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 protocol criteria.
• Provide medical oversight for trial participants including safety assessments and ongoing care.
• Collaborate with CRCs, Sponsors, and Monitors to ensure protocol compliance and data integrity.
• Review and sign off on source documents, CRFs, and regulatory documentation.

Skills

Endocrinology

Clinical research oversight

GCP certification

EMR/CTMS proficiency

Communication skills

Education

MD or DO

Tools

EMRs

CTMS

Job description

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).