Research Coordinator I - Surgery

Manage clinical trial operations by scheduling appointments, preparing subject visits, and performing data entry in the Clinical Trial Management System and Electronic Data Capture tools. Compile and maintain essential regulatory documents for IRB submissions and sponsor communications while tracking study records and ensuring compliance with ICH GCP guidelines. Safeguard participant safety by adhering to ethical research principles, investigating incomplete data, and maintaining accurate Case Report Forms. Assist with site visit coordination, document management, and participating in manuscript development under direct supervision.