Clinical Specialist
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Job Description
- Demonstrate proficiency and understanding of all aspects of the approved DurAVR clinical trial protocol, including inclusion & exclusion criteria, and accuracy in obtaining any required imaging and pre & post procedural data.
- Demonstrate proficiency in pre-case planning, CT analysis and pre & post procedure recommendations to ensure optimal clinical outcomes.
- In-depth knowledge and understanding of existing DurAVR clinical data as well as all competitive TAVI data.
- Support the Clinical & Regulatory Operations team, assisting with site communications, data compliance activity, screening review efficiency and site submission efficiency.
Employment Type
Remote
Department / Functional Area
Administration
Key Skills
- Management
