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Care Access is seeking a Clinical Research Coordinator III in Tampa, United States, to oversee complex clinical research protocols while ensuring compliance with Good Clinical Practices. The ideal candidate will have significant experience in clinical research, excellent organizational skills, and be bilingual in Spanish.
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Job Summary
The Clinical Research Coordinator’s primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
The CRC III is responsible for the most pivotal and complex protocols and study designs being conducted at Care Access Research sites.
Responsible for mentoring and training CRAs and CRC I/CRC II to ensure complete understanding of Care Access processes, SOPs, and values.
Matching Summary
Match Score: 75
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Care Access is seeking a Clinical Research Coordinator III in Tampa, United States, to oversee complex clinical research protocols while ensuring compliance with Good Clinical Practices. The ideal candidate will have significant experience in clinical research, excellent organizational skills, and be bilingual in Spanish.
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Skills & Requirements
Must-have
Good Clinical Practices (GCP)
protocol and regulatory compliance
patient screening and enrollment
informed consent process
adverse event identification
electronic data capture (EDC)
sponsor and CRO interaction
Nice-to-have
patient experience and safety
positive, professional manner
continuous independent learning
leading corrective actions
Key Requirements
Bilingual in Spanish required
Minimum of 5 years prior Clinical Research Coordinator experience