Project Coordinator

Job Summary

Supporting the Clinical Trials Office, the full-time Project Coordinator will manage administrative and regulatory tasks for research studies, ensuring efficient meeting coordination and compliance with institutional policies while working remotely.

Key responsibilities

• Coordinate and schedule meetings for the D/M Team, ensuring proper format and distribution of agendas and minutes
• Manage regulatory documents and maintain completeness of regulatory files for assigned trials
• Serve as the primary contact for study status inquiries and assist in the initiation and close-out of studies

Required qualifications

• Bachelor's Degree or an AD/GED with 2 years of clerical or similar experience
• Preferred knowledge of Clinical Research and regulatory forms
• Experience with clinical trials management systems (CTMS) is advantageous