Study Coordinator

Job Summary

To support remote site activities for assigned projects, the part-time Study Coordinator will manage day-to-day communications, assist with subject recruitment and re-consenting, and maintain compliance documentation while residing in or near Winter Park, FLA.

Key responsibilities

• Serve as the primary contact for site communications and activity coordination
• Support recruitment activities and manage subject re-consenting and medical record acquisition
• Perform data entry and monitor clinical databases while ensuring compliance with IRB/FDA policies

Required qualifications

• Bachelor's degree or equivalent experience with a minimum of 2 years in a related field
• Current knowledge of ICH/GCP and applicable regulations and guidelines
• Experience with web-based research platforms and clinical databases
• Ability to work independently and collaboratively with other team members
• Strong organizational skills and the ability to multitask effectively