Hybrid Clinical Research Coordinator III — Training & Compliance

The University of Pittsburgh; Pittsburgh (Allegheny County); Hybrid; USD 49,000 - 69,000; Full time

Job summary

The University of Pittsburgh invites applications for a Clinical Research Coordinator III to support clinical trials at the Pittsburgh campus. The role focuses on coordinating site communications, training staff, and assisting with IRB submissions.

Ideal candidates will have a Master\'s degree, at least one year of experience, strong organizational skills, and the ability to manage budgets and study documentation. Hybrid work arrangement will balance on-site and remote duties.

Qualifications

• Master's degree required.
• Minimum 1 year of experience in clinical research or related field.
• Experience with IRB submissions and study documentation is preferred.

Responsibilities

• Coordinate clinical site communications and monitor site operations.
• Develop and deliver site personnel training and certification.
• Assist with IRB submissions and regulatory documentation.
• Prepare reports and assist with study budget tracking.
• Lead team meetings and monitor data collection and study recruitment plans.

Skills

Project management

Organizational skills

Attention to detail

Education

Master's degree

Job description

The University of Pittsburgh invites applications for a Clinical Research Coordinator III to support clinical trials at the Pittsburgh campus. The role focuses on coordinating site communications, training staff, and assisting with IRB submissions.

Ideal candidates will have a Master\'s degree, at least one year of experience, strong organizational skills, and the ability to manage budgets and study documentation. Hybrid work arrangement will balance on-site and remote duties.