Clinical Research Associate- Part Time (20 hrs)- Day Shift

General Summary

Responsibilities

• Plans, organizes, performs and monitors daily project protocols.
• Collections, 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.
• Affords assistance with the preparation and delivery of internal and external presentations, conference reports and lectures, and publishing submissions.

Requirements

• Understanding of the Food and Drug Administration (FDA) rules is beneficial.

Education/Experience

• 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: Not Applicable
• Union Code: Not Applicable