Project Coordinator

Job Summary

To support the Clinical Trials Office, the part-time Project Coordinator will manage administrative and regulatory duties, coordinate meetings, and ensure compliance with institutional policies while working remotely.

Key responsibilities

• Schedule and coordinate D/M Team meetings, ensuring proper format and resources are in place
• Manage regulatory documents and maintain regulatory files for assigned trials
• Serve as the primary contact for status inquiries on new studies and coordinate study initiation and close-out visits

Required qualifications

• Bachelor's Degree or an Associate Degree/GED with 2 years of clerical or similar experience
• Preferred education includes a BA/BS degree
• Knowledge of Clinical Research and regulatory forms is preferred