Endocrinologist - Clinical Research Investigator

ECN Clinical; Long Beach (CA); On-site; USD 120,000 - 180,000; Part time

Job summary

ECN Clinical seeks an Endocrinologist to serve as Principal Investigator or Sub-Investigator on multiple Phase I–IV trials while continuing to provide adult patient care in a clinical research setting. This part-time/per diem position offers meaningful opportunities to advance medicine through dedicated trial oversight.

You will perform physical exams, assess eligibility, monitor safety, ensure protocol compliance, and collaborate with sponsors, monitors, and coordinators.

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.
• GCP certification or willingness to obtain prior to start.
• Minimum of 1 year of clinical practice; prior clinical research experience preferred.

Responsibilities

• Serve as Principal Investigator or Sub-Investigator on multiple Phase I–IV clinical trials.
• Perform comprehensive physical exams and assessments for protocol screening.
• Evaluate patient eligibility based on inclusion/exclusion criteria.
• Provide medical oversight for trial participants, including safety assessments.
• Collaborate with coordinators, sponsors, and monitors for protocol compliance and data integrity.
• Review and sign source documents, CRFs, and regulatory documentation.
• Maintain trial documentation per ICH-GCP, FDA, and sponsor requirements.
• Participate in Site Initiation Visits, Monitoring Visits, and Audits.

Skills

Attention to detail

Communication skills

Team collaboration

EMR familiarity

Education

MD or DO degree from an accredited medical school

Valid medical license in state of employment

Board Certified/Eligible in Endocrinology

GCP certification

Tools

EMR systems

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).