Which coordinator monitors the quality of cancer registry data?

The Cancer Registry Quality Coordinator is specifically responsible for monitoring and ensuring the quality of cancer registry data. This role involves overseeing the accuracy, completeness, and timeliness of data collected in the cancer registry, which is crucial for tracking cancer incidence, treatment outcomes, and patient demographics.

The coordinator engages in regular audits to identify discrepancies, provides training for staff on data collection processes, and ensures compliance with regulatory standards set by organizations such as the Commission on Cancer (CoC). By maintaining high-quality data, the Cancer Registry Quality Coordinator plays a critical role in enabling healthcare providers and researchers to make informed decisions related to cancer care and treatment strategies.

In contrast, the Clinical Research Coordinator typically focuses on managing clinical trials and research projects, the Community Outreach Coordinator works to promote cancer awareness and prevention within the community, and the Psychosocial Services Coordinator addresses the psychological and social needs of cancer patients. None of these roles specifically involve monitoring cancer registry data.