Role OverviewThe Clinical Research Coordinator II will work with populations at risk for bloodborne pathogens and sexually transmitted infections (STIs), processing and preparing blood and urogenital specimens for delivery to a research laboratory. The position will be responsible for coordinating and conducting procedures for clinical research studies, including participant recruitment, consent, data collection, and study visit scheduling.
What You Will Do
The CRC II will be responsible for coordinating and conducting procedures for clinical research studies, including participant recruitment, consent, data collection, and study visit scheduling. They will also participate in other research-related activities, such as data verification, IRB submissions, and study close-outs.
Why It Might Be a Fit
The ideal candidate will have clinical research experience, clinical study project management experience, and experience with UAB's internal systems (IRAP, IRB, CIRB, etc.).
Requirements
- Bachelor's degree in a related field
- Three (3) years of related experience
- Clinical research experience
- Clinical study project management experience
- Experience with UAB's internal systems (IRAP, IRB, CIRB, etc.)
Benefits
- Annual Salary Range: $50,050 - $65,000
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