- Terumo Medical Corporation (Elkton, MD)
- Adverse Event Reporting Spec II Date: Nov 14, 2025 Req ID: 5335 Location: Elkton, MD, US Company: Terumo Medical Corporation Department: Post Market ... US and global health authorities (GHA) such as FDA, HC, MHRA, etc. The Adverse Event Reporting Team is responsible with implementation of best practices to… more
- University of Rochester (Rochester, NY)
- …procedures, study activities, source documentation and case report form (CRFs) completion, and adverse event reporting . + Reviews and documents the ... use of device, and/or other interventional activities, to document adverse events and report to senior study staff, PI,...questions that arise during the study, communicates and documents adverse events as advised by the PI and ensures… more