Pediatric Clinical Trials Coordinator

Yale University; New Haven (CT); On-site; USD 65,000 - 101,000; Full time

Job summary

Yale University is seeking a Research Coordinator to manage TrialNet clinical trials and other pediatric type 1 diabetes studies. You will handle study performance, regulatory documents, data entry, and participant follow-up in a collaborative team.

The role involves recruiting families, coordinating scheduling, and ensuring high-quality data management while traveling between Yale sites as needed. A Bachelor’s degree with relevant experience is required.

Qualifications

• Experience with clinical trials and ability to communicate with participants and families.
• Excellent organizational skills and attention to detail.
• Willingness to travel between Yale School of Medicine and affiliated sites.
• Experience with data collection and database management is a plus.

Responsibilities

• Assumes primary responsibility for a program, service, activity, operation or function in an assigned area. Develops objectives, practice and procedure and identifies resources to ensure accomplishment of operational goals.
• Coordinates day-to-day operations in order to achieve designated goals. Ensures effective management and leads the development and implementation of best practices.
• Designs and implements quality control metrics to identify areas of risk. Analyzes, recommends, and implements strategic solutions to minimize risk.
• Develops a variety of complex report and other written materials.
• Provides guidance to and collaboration with internal and external partners as necessary.
• Develops, oversees and monitors budgets.
• Develops and maintains specialized training.
• Performs other duties as assigned.

Skills

Clinical research coordination

Participant communication

Organizational skills

Team collaboration

Independent work

Education

Bachelor’s Degree in related field

Job description

Yale University is seeking a Research Coordinator to manage TrialNet clinical trials and other pediatric type 1 diabetes studies. You will handle study performance, regulatory documents, data entry, and participant follow-up in a collaborative team.

The role involves recruiting families, coordinating scheduling, and ensuring high-quality data management while traveling between Yale sites as needed. A Bachelor’s degree with relevant experience is required.