Endocrinologist - Clinical Research Investigator

Elite Clinical Network; Long Beach (CA); On-site; USD 130,000 - 145,000; Part time

Job summary

A leading clinical research organization in California is seeking a part-time Physician – Endocrinologist to oversee clinical trials and provide medical care to patients. This role involves serving as Principal Investigator or Sub-Investigator, conducting patient assessments, and ensuring protocol compliance. Ideal candidates will have a medical degree, be board certified in Endocrinology, and possess strong communication skills. This position offers a competitive salary ranging from $130,000 to $145,000 annually.

Qualifications

• MD or DO degree from an accredited medical school.
• Valid, unrestricted medical license in the state of employment.
• Minimum of 1 year of experience in clinical practice.

Responsibilities

• Serve as Principal Investigator or Sub‑Investigator on clinical trials.
• Perform comprehensive physical exams and clinical assessments.
• Evaluate patient eligibility based on clinical protocols.

Skills

Attention to detail

Interpersonal skills

Communication skills

Experience in clinical research

Familiarity with FDA and ICH-GCP

Education

MD or DO degree

Board Certified or Board Eligible in Endocrinology

Current Good Clinical Practice (GCP) certification

Job description

Position Overview

Elite Clinical Network (ECN) is seeking a dedicated and research-oriented Physician – Endocrinologist 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).
• DEA license (preferred).

Job Details

• Seniority level: Mid‑Senior level
• Employment type: Part‑time
• Job function: Strategy/Planning and Information Technology
• Location: Los Angeles, CA
• Salary: $130,000.00 – $145,000.00 (annual)
• Shift: Part‑time / per diem, clinical research setting.