Endocrinologist - Clinical Research Investigator

Elite Clinical Network; Carrollton (TX); On-site; USD 120,000 - 180,000; Part time

Job summary

A clinical research organization is seeking a dedicated Physician – Endocrinologist to join their expanding team. This part-time position involves serving as a Principal Investigator or Sub-Investigator on clinical trials while ensuring high-quality medical care to patients. The ideal candidate will have an MD or DO degree, a valid medical license in Texas, and experience in clinical practice. Strong communication and collaboration skills are essential for this role, alongside a commitment to advancing medical research.

Qualifications

• Board Certified or Board Eligible in Endocrinology.
• Valid, unrestricted medical license in Texas required.
• Minimum of 1 year of clinical practice experience.
• GCP certification or willingness to obtain before start.

Responsibilities

• Serve as Principal Investigator or Sub-Investigator on clinical trials.
• Perform physical exams and clinical assessments.
• Evaluate patient eligibility for protocols.
• Collaborate with coordinators, sponsors, and monitors to ensure compliance and data integrity.
• Review source documents, CRFs, and regulatory paperwork; maintain trial documentation.

Skills

Attention to detail

Patient communication

Collaboration

Medical license

EMR/CTMS proficiency

Data integrity

Education

MD or DO degree

Current GCP certification

Tools

Electronic medical records (EMRs)

Clinical trial management systems (CTMS)

Job description

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.

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).