On-Site Study Coordinator

Job Summary

Supporting remote site activities, the part-time On-Site Study Coordinator will manage day-to-day site communications, assist with subject recruitment, and ensure compliance with regulatory documentation.

Key responsibilities

• Serve as the main point of contact for site communications and document submissions
• Assist with subject re-consenting, medical record acquisition, and protocol activities as directed by the Principal Investigator
• Perform data entry and monitor clinical databases while maintaining compliance with IRB/FDA policies

Required qualifications

• Bachelor's degree or equivalent experience with a minimum of 2 years of study coordinator experience
• Experience in study team roles is ideal
• Current knowledge of ICH/GCP and applicable regulations
• Ability to manage technology and web-based research platforms
• Strong organizational skills and ability to multitask effectively