Follow applicable departmental Standard Operating Procedures and Work Instructions.
Complete required trainings according to timelines.
Review and action queries on an ongoing basis and update database appropriately in accordance with Global Data Management Plans and applicable standardized data management.
Perform UAT according to Validation Plan for applicable Data Management systems (if applicable).
Generate, resolve and track queries to address inconsistent data identified during data review activities and apply proper modification / correction to the database.
Run ancillary programs (e.g., diagnostics, special listings, reconciliation discrepancy listings) used to support the review of clinical trial data.
Review reports and take actions as defined in the DMP or eCRF review manual.
Assist with the review of clinical data by patient, site and / or project to identify data inconsistencies that require further investigation.
Involve in data management system edit / data validation checks and special listings / procedures used as tools for the data review and discrepancy management activities.
Maintain Data Management related operational data flows.
Ensure that all Data Management activities are conducted in compliance with relevant regulatory requirements.
Other duties as assigned by study management.
1-2 years of relevant DM experience
Sorry the Share function is not working properly at this moment. Please refresh the page and try again later.
Share on your newsfeed