Clinical Programs Coordinator

studenttechnology.yale.edu

New Haven, Connecticut, US
$65,000.00 - $101,000.00; not specified; not speci...
Clinical trial management
Human subjects regulations
Data management systems
The Clinical Programs Manager will oversee and coordinate key clinical initiatives within the Department of Ophthalmology and Visual Science, with a primary focus on managing the department’s clinical trial programs and leading the coordination of the Retinopathy of Prematurity (ROP) program

Job Summary

  • The Clinical Programs Manager will oversee and coordinate key clinical initiatives within the Department of Ophthalmology and Visual Science, with a primary focus on managing the department’s clinical trial programs and leading the coordination of the Retinopathy of Prematurity (ROP) program.
  • This position serves as a central resource for coordinating all aspects of the clinical research operations and programmatic alignment, ensuring that both clinical trials and ROP coordination activities are conducted efficiently, in compliance with institutional and regulatory standards, and in collaboration with faculty, research staff, hospital partners, and external stakeholders.
  • Working at Yale means contributing to a better tomorrow. Whether you are a current resident of our New Haven-based community- eligible for opportunities through the New Haven Hiring Initiative or a newcomer, interested in exploring all that Yale has to offer, your talents and contributions are welcome.

Matching Summary

The Clinical Programs Manager will oversee and coordinate key clinical initiatives within the Department of Ophthalmology and Visual Science, with a primary focus on managing the department’s clinical trial programs and leading the coordination of the Retinopathy of Prematurity (ROP) program.

Salary

$65,000.00 - $101,000.00; Not specified; Not specified

Skills & Requirements

Must-have

  • Clinical trial management
  • Human subjects regulations
  • Data management systems
  • Multi-site studies coordination
  • HIC/IRB submissions

Nice-to-have

  • Patient recruitment processes
  • Statistical analysis software
  • Neonatal ophthalmology coordination
  • Work collaboratively across disciplines

Key Requirements

  • Master’s Degree or equivalent experience
  • Two years of experience
  • Clinical research regulations knowledge
  • GCP and IRB processes experience
  • Informed consent ability
  • Manage multiple concurrent projects
  • Microsoft Suite proficiency
  • OnCore, Workday, or Epic proficiency

Work Rights

Not specified

Tailored Resume

Cover Letter