Role OverviewThe Clinical/Translational Research Coordinator II is responsible for coordinating the approval processes and conduct of research protocols, ensuring the integrity and quality of the clinical/translational research.
What You Will Do
The coordinator will prepare and process new IRB research proposals, amendments, continuing review applications, and adverse event reports, as well as participate in site visits and ensure research information is collected and stored in a compliant manner.
Why It Might Be a Fit
The role requires a strong understanding of research regulations and policies, as well as excellent communication and organizational skills to effectively coordinate research protocols and ensure the integrity of the research.
Requirements
- Certifications
- Work Experience
- Relevant Work Experience
- Experience Level
- Education
Benefits
- health
- disability
- retirement
- wellness
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