Description JOB SUMMARY: With guidance and training, this position is primarily responsible for overseeing the development of the VUMC Heart Valve Registry as well as Industry Sponsored Heart Valve Clinical Trials, in accordance with Good Clinical Practice Guidelines and Vanderbilt Policy and Procedures. Essential tasks for this role will include regular participant interaction, consenting, survey administration, specimen collection, large/complex database management, data entry surrounding participant procedures, accurate and timely documentation, regulatory maintenance, tracking follow-up appointments, etc. A secondary responsibility will involve assisting with the enrollment and study visits for patients included in industry-supported device trials o