Clinical Research Associate- Contingent- Day Shift (8:15-6:30p)

Candidate must be willing to work one day a week (Tuesday, Wednesday, or Thursday, 8:15 AM–6:30 PM) and every other Saturday (10 AM or 11 AM start time for 3 hours).

About the Role

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, lectures, and publishing submissions.

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

Requirements

• High School diploma or equivalency with 2 years of cumulative experience OR
• Associate degree/Technical degree OR
• 4 years of applicable cumulative job-specific experience.

Organization: Henry Ford Health St. John Hospital
Department: Cord Blood Collection Program
Shift: Day Job