Endocrinologist - Clinical Research Investigator

ECN Clinical; Carrollton (TX); On-site; USD 100,000 - 170,000; Part time

Job summary

ECN Clinical seeks an Endocrinologist to join as a Clinical Research Investigator, potentially as Principal Investigator or Sub-Investigator, in a per diem, part-time capacity. The role blends high-quality medical care with oversight of adult participants in clinical trials.

You will ensure protocol compliance and data integrity while guiding patient safety in a dynamic research setting. The candidate should hold an MD/DO with an unrestricted TX license, be BC/BE in Endocrinology (or BC/BE in

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

Responsibilities

• Serve as PI or Sub-Investigator on Phase I–IV trials.
• Perform physical exams and protocol screening for enrollment.
• Evaluate eligibility based on protocol criteria.
• Provide medical oversight and safety assessments for participants.
• Collaborate with coordinators, sponsors, and monitors for compliance.
• Sign source documents, CRFs, and regulatory paperwork.
• Maintain trial documentation per ICH-GCP, FDA, sponsor rules.
• Participate in SIVs, monitoring visits, and audits.
• Manage chronic/acute conditions per study guidelines.
• Educate patients on procedures, consent, and side effects.

Skills

Clinical Trials

EMR/CTMS

Patient Care

Communication

Education

MD/DO

Medical license (TX)

BC/BE in Endocrinology

GCP Certification

Endocrinology fellowship

Tools

EMR Systems

CTMS

Job description

Endocrinologist -Clinical Research Investigator

ECN Clinical is seeking a dedicated and research-oriented Endocrinologist - Clinical Research Investigatorto 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).