Clinical Research Associate - Cardiology - 40 hours/week - Southfield
Southfield, MIPosted Apr 4, 2026
Behavioral Health Market Context
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Job Description
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• 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 Providence Hospitals
• Shift: Day Job
• Union Code: Not Applicable
• 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 Providence Hospitals
• Shift: Day Job
• Union Code: Not Applicable
Qualifications
- •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
Benefits
Responsibilities
- •Participates in the design, administration and monitoring of clinical trials
- •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