Clinical Research Associate - 24 hrs/wk - Days - Southfield

GENERAL SUMMARY:

Participates in the design, administration and monitoring of clinical trials. Responsibilities: Plans, organizes, performs and monitors daily project protocols.| Collects, prepares and maintains required research documentation, such as informed consent records, case records, clinical notes and medical reports.| Reports and assists with the management of protocol deviations, adverse events and other project-related issues.| Assists with the preparation and delivery of internal and external presentations, conference reports and lectures, and publishing submissions.| Understanding of the Food and Drug Administration (FDA) rules is beneficial.