To support clinical research efforts, the full-time Data Coordinator II will be responsible for collecting, processing, and ensuring the quality of clinical trial data while collaborating with research teams and maintaining databases, with the option for remote work. Key responsibilities Collect, abstract, and code complex clinical data from various sources for research subjects Maintain databases and resolve data queries with minimal errors Track and manage research subject schedules based on protocol-specific requirements Required qualifications BA/BS, RRA, ART, or a two-year degree in the medical field Two years of experience in medical records, cancer registry, or a related field Strong computer skills with experience in database management Familiarity with medical terminology