Endocrinologist - Clinical Research Investigator

Elite Clinical Network; North Las Vegas (NV); On-site; USD 150,000 - 200,000; Part time

Job summary

Elite Clinical Network is looking for a dedicated Physician – Endocrinologist to join their team in North Las Vegas, NV. This part-time position requires an MD or DO degree, with responsibilities as a Principal Investigator or Sub-Investigator on clinical trials. Candidates should possess a valid medical license and be Board Certified or Board Eligible in Endocrinology. The role includes evaluating patient eligibility, providing oversight for participants, and ensuring compliance with protocols and regulations.

Qualifications

• Minimum of 1 year of experience in clinical practice.
• Valid, unrestricted medical license in Nevada.
• Familiarity with FDA and ICH-GCP protocols.

Responsibilities

• Serve as Principal Investigator or Sub-Investigator on multiple clinical trials.
• Evaluate patient eligibility and provide medical oversight.
• Manage chronic and acute conditions among study participants.

Skills

Attention to detail

Interpersonal skills

Communication skills

Collaboration

Education

MD or DO degree from an accredited medical school

Board Certified or Board Eligible in Endocrinology

Current Good Clinical Practice (GCP) certification

Tools

Electronic medical records (EMRs)

Clinical trial management systems (CTMS)

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).