Clinical Data Specialist

Review clinical trial data in accordance with Data Management Plans and applicable standardized data management processes (SOPs; Work Instructions, etc.) to identify erroneous, missing, incomplete, or implausible data.Run ancillary programs (e.g., diagnostics, special listings, reconciliation discrepancy listings) used to support the review of clinical trial data.Generate, resolve and track queries to address problematic data identified during data review activities and apply proper modification / correction to database.Apply quality control procedures and checks to ensure data quality standards (Client and LabCorp) are achieved.Interact with the dictionary coding and maintenance group to ensure appropriate process set up and application.Assist with Reconciliation of central laboratory and / or third party vendor data (eCRF, edDiary, specialty laboratory, etc.).Assist with aggregate review of clinical data by patient, site and / or project to identify data trend, (patient safety, compliance, etc.) and / or data inconsistencies that require further investigation.Assist in the development and testing of data management system edit/ data validation checks (diagnostics) and special listings / procedures used as tools for the data review and discrepancy management activities.Support the training of project staff on project-specific, global, standardized data management processes.Perform the duties as assigned by management. Labcorp is proud to be an Equal Opportunity Employer: As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status. For more information about how we collect and store your personal data, please see our Privacy Statement.