- Gain in-depth knowledge of FDA approved and investigational OrganOx products and clinical procedures.
- Support the development of training materials for approved and research-stage devices.
- Train research centers and internal personnel on study protocols and device operation.
- Attend clinical cases to provide technical and clinical resource support.
- Collaborate with development and engineering teams to provide technical feedback and address design queries.
- Assist in the design and implementation of study-specific databases and support data collection/review.
- Contribute to the writing and review of clinical study reports and FDA regulatory submissions.