Clinical Research Coordinator — Pulmonary Trials & Data

University-of-North-Carolina-At-Chapel-Hil; Eastowne (NC); On-site; USD 52,000 - 70,000; Full time

Benefits offered by this job

Comprehensive benefits package

Job summary

University of North Carolina at Chapel Hill is seeking an Associate Clinical Research Coordinator in the Department of Medicine, Division of Pulmonary Diseases and Critical Care Medicine. The role supports execution of clinical research protocols, regulatory tasks, recruitment, informed consent, and data management for multiple studies at the Chapel Hill campus.

This on-site position may include evening hours and requires a Bachelor’s degree or equivalent, with knowledge of Good Clinical

Qualifications

• Knowledge of Good Clinical Practice (GCP) and regulatory standards.
• Experience coordinating IRB submissions and study documents.
• Ability to collect, manage and report clinical data accurately.

Responsibilities

• Execute and monitor clinical research protocols across studies.
• Assist with recruitment, informed consent, and participant scheduling.
• Maintain regulatory documentation and ensure data integrity and compliance.

Skills

Clinical research

IRB submissions

Education

Bachelor’s degree

Job description

University of North Carolina at Chapel Hill is seeking an Associate Clinical Research Coordinator in the Department of Medicine, Division of Pulmonary Diseases and Critical Care Medicine. The role supports execution of clinical research protocols, regulatory tasks, recruitment, informed consent, and data management for multiple studies at the Chapel Hill campus.

This on-site position may include evening hours and requires a Bachelor’s degree or equivalent, with knowledge of Good Clinical