Clinical Research Associate

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.
EDUCATION/EXPERIENCE REQUIRED:

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.
Additional Information
Organization: Henry Ford Health St. John Hospital
Department: Cord Blood Collection Program
Shift: Day Job
Union Code: Not Applicable