Prepares and submits regulatory submission to IRB and sponsors, documentation compliance for multiple study projects, audit preparation, and data submission. This position also will be responsible for advising patients of trial design, facilitating informed consent for investigators, following strict adherence to protocol procedures specific to each study, screening for possible trial patients, eligibility criteria, and patient follow up. This position is responsible for coordination of trial activities mentioned above, as well as, others.

- Require graduation from a Cardiovascular Technology Program.
- Require completion of the following training programs within thirty (30) days of hire: Good Clinical Practice; Human Subject Protection; & Safe Handling/Hazardous
- Require a minimum of five (5) years of healthcare experience preferably with previ...