<p>GENERAL SUMMARY</p> <p>Location: Henry Ford Providence Southfield Hospital</p> <p>Cardiology Unit</p> <p>Participates in the design, administration and monitoring of clinical trials.</p> <p>Responsibilities</p> <ul> <li>Plans, organizes, performs and monitors daily project protocols. </li><li>Collects, prepares and maintains required research documentation, such as informed consent records, case records, clinical notes and medical reports. </li><li>Reports and assists with the management of protocol deviations, adverse events and other project-related issues. </li><li>Assists with the preparation and delivery of internal and external presentations, conference reports and lectures, and publishing submissions. </li><li>Understanding of the Food and Drug Administration (FDA) rules is beneficial. </li></ul> <p>EDUCATION/EXPERIENCE REQUIRED</p> <p>High School diploma equivalency with 2 years of cumulative experience OR Associate degree/Technical degree OR 4 years of applicable cumulative job specific experience required.</p> <p>Additional Information</p> <ul> <li>Organization: Henry Ford Providence Hospitals </li><li>Shift: Day Job </li><li>Union Code: Not Applicable </li></ul>