The Clinical Research Coordinator II (CRC II) procures, processes and ships research specimens and conducts patient recruitment/consenting, administers questionnaires, abstracts medical records, maintains patient databases, enters data into sponsor-specific electronic data capture forms, performs administrative tasks, assists in grant preparation, participates in preparation of data and other reports and assists with audits, quality improvement projects, and CH-CRP patient and community engagement efforts.
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Job Type
Full-time
Career Level
Mid Level