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Clinical Data Professionals (2-8 years)

Laboratory Corporation of America Holdings (Covance)

Bangalore, India

<h2>Job Overview:</h2><p style="margin: 0in 0in 0.2pt 17.25pt;"> </p><p style="margin: 0in 0in 0.2pt 17.25pt;"><span style="font-family: calibri, sans-serif; font-size: 10pt;">Review clinical trial data in accordance with [Global] Data Management Plans and applicable standardized data management processes (SOPs; Work Instructions, etc.) to identify erroneous, missing, incomplete, or implausible data.</span></p><p style="margin: 0in 0in 0.2pt 0.25in;"><span style="font-family: calibri, sans-serif; font-size: 10pt;">Run ancillary programs (e.g., diagnostics, special listings, reconciliation discrepancy listings) used to support the review of clinical trial data.</span></p><ol><ol><li style="color: black;"><span style="font-family: calibri, sans-serif; font-size: 10pt;">Generate, resolve and track queries to address problematic data identified during data review activities and apply proper modification / correction to the database.Interact with the dictionary coding and maintenance group to ensure appropriate process set-up and application.</span></li><li style="color: black; font-family: 'Times New Roman',serif; font-size: 11pt; margin-top: 0in; margin-bottom: 0.2pt;"><span style="font-family: calibri, sans-serif; font-size: 10pt;">Assist with the reconciliation of central laboratory and / or third party vendor data (eCRF, edDiary, specialty laboratory, etc.).</span></li><li style="color: black; font-family: 'Times New Roman',serif; font-size: 11pt; margin-top: 0in; margin-bottom: 0.2pt;"><span style="font-family: calibri, sans-serif; font-size: 10pt;">Apply quality control procedures and checks to ensure data quality standards (client and Labcorp) are achieved.</span></li><li style="color: black; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-family: calibri, sans-serif; font-size: 10pt;">Assist with the aggregate review of clinical data by patient, site and/ or project to identify data trends (patient safety, compliance, etc.) and / or data inconsistencies that require fulther investigation.Suppolt the training of project staff on project-specific, global, standardized data management processes.</span></li><li style="color: black; font-family: 'Times New Roman',serif; font-size: 11pt; margin-top: 0in; margin-bottom: 0.2pt;"><span style="font-family: calibri, sans-serif; font-size: 10pt;">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.</span></li><li style="color: black; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-family: calibri, sans-serif; font-size: 10pt;">Perform other duties as assigned by management.</span></li></ol></ol><h2>Education/Qualifications:</h2><ul><li><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Msc/Bsc in Life Science</span></li></ul><h2>Experience:</h2><ul><li><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">2-8 years of relevant Clinical Data Management experience.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Position opened at various levels.</span></li></ul>

Job posted: 2021-12-23

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