Clinical Research Associate Contingent- Covering both Novi & Southfield Campuses

GENERAL SUMMARY

Department: Research

CONTINGENT- Covering both Novi & Southfield Campuses

Monday - Friday 7:00am - 3:30pm- no weekends

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.