Part-Time Endocrinologist | Clinical Research Investigator

ECN Clinical; Denver (CO); Vor Ort; USD 124.000 - 207.000; Teilzeit

Zusammenfassung

ECN Clinical is seeking an Endocrinologist for a part-time per diem role as a Clinical Research Investigator. You will serve as a Principal Investigator or Sub-Investigator on Phase I–IV trials, oversee patient evaluations, and ensure protocol compliance in a clinical research setting.

The role emphasizes medical oversight, informed consent, safety monitoring, and collaboration with sponsors and study teams. Prior GCP experience is preferred and licensure is required.

Qualifikationen

• MD or DO degree
• Unrestricted medical license in the state of employment
• Board Certified or Board Eligible in Endocrinology
• BC/BE in Family Medicine or Geriatric Medicine also considered
• Current Good Clinical Practice (GCP) certification or willing to obtain before start
• Minimum 1 year of clinical practice; clinical research exp preferred but not required

Aufgaben

• Serve as Principal Investigator or Sub-Investigator on multiple Phase I–IV trials.
• Perform comprehensive physical exams and protocol screening/enrollment assessments.
• Evaluate patient eligibility based on inclusion/exclusion criteria.
• Provide medical oversight and safety assessments for trial participants.
• Collaborate with CR Coordinators, Sponsors, and Monitors for protocol compliance and data integrity.
• Review and sign source documents, CRFs, and regulatory paperwork.

Kenntnisse

Attention to detail

Communication skills

Team collaboration

EMR/CTMS experience

Clinical research acuity

Ausbildung

MD or DO degree

Unrestricted medical license (state)

Board Certified/Eligible in Endocrinology

BC/BE in Family Medicine or Geriatric Medicine considered

GCP certification

1 year clinical practice

Jobbeschreibung

ECN Clinical is seeking an Endocrinologist for a part-time per diem role as a Clinical Research Investigator. You will serve as a Principal Investigator or Sub-Investigator on Phase I–IV trials, oversee patient evaluations, and ensure protocol compliance in a clinical research setting.

The role emphasizes medical oversight, informed consent, safety monitoring, and collaboration with sponsors and study teams. Prior GCP experience is preferred and licensure is required.