ECN Operating LLC

Compensation

Full 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 Endocrinologist. • 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).