Clinical Data Associate Full-time Job

Responsible for supporting the collection, management, and analysis of clinical trial data. The role may involve tasks such as reviewing study protocols and case report forms, verifying data accuracy, conducting database reconciliation, and generating study reports. Additionally, the Clinical Data Associate may be responsible for ensuring data quality, preparing data for statistical analysis, and working with the study team to resolve data-related issues. Ensure that all Data Management activities are conducted in compliance with Good Clinical Practice guidelines. Complete required trainings according to timelines. Review and action queries on an ongoing basis and update database appropriately in accordance with Data Management Plans (DMP) and applicable standardized data management tasks, as assigned. Perform UAT according to Validation Plan for applicable Data Management systems (if applicable). Good attention to detail, strong organizational skills, and the ability to work effectively in a team environment are also important. Familiarity with clinical trial processes and regulations, as well as experience with data management and analysis, is a plus.