Clinical Research Coordinator I - Hemostasis Treatment Center

What you’d do

Coordinate clinical research protocols at the Hemostasis Treatment Center, including preparing IRB submissions, maintaining regulatory documents, and supporting sponsor site visits. Full time. Found on the employer's careers page on Oct 8, 2026. Apply through the link.

You’ll need

• Experience with IRB submissions and amendments
• Knowledge of federal research regulations
• Clinical research documentation and source records
• Regulatory compliance and adverse event reporting