Role OverviewThe Clinical Translational Research Coordinator II demonstrates comprehensive expertise in the coordination and management of clinical and translational research studies while ensuring compliance with institutional policies, federal regulations, Good Clinical Practice (GCP), and human subject protection requirements.
What You Will Do
Key responsibilities include preparing and submitting regulatory documents, maintaining essential regulatory documentation, coordinating study operations, screening and recruiting participants, managing clinical research data, and supporting sponsor monitoring visits.
Why It Might Be a Fit
This role requires a strong understanding of clinical trial management, regulatory affairs, and human subjects protection, with a focus on ensuring participant safety and regulatory compliance.
Requirements
- Certifications
- Work Experience
- Bachelor's degree
Benefits
- health
- disability
- retirement
- wellness
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