Oversee the entire Clinical Trial Data Management process, from start-up to database lock, ensuring data quality, accuracy, and compliance with regulations Contribute to the development of project timelines and resource planning. Develop training materials and documentation for internal users and site personnel Design and Implement detailed data management plans (DMPs) and data collection strategies that covers coding, data transfer, discrepancy management, workflow, reporting, and data validation. Develop, configure, and verify clinical databases and electronic data capture (EDC) systems, including case report forms (CRFs). Generate and review Data cleaning listings such as offline listings, medical coding listings and missing pages reports. o Conduct data entry, cleaning, validation checks, and resolve discrepancies to uphold data accuracy, completeness, and compliance with quality standards. Collaborate with cross-functional study teams to resolve data-related issues, integrate feedback, and align data management practices with study protocols. o Adhere to Good Clinical Practice (GCP) and CDISC standards. Oversee the entire Clinical Trial Data Management process, from start-up to database lock, ensuring data quality, accuracy, and compliance with regulations Contribute to the development of project timelines and resource planning. Develop training materials and documentation for internal users and site personnel Design and Implement detailed data management plans (DMPs) and data collection strategies that covers coding, data transfer, discrepancy management, workflow, reporting, and data validation. Develop, configure, and verify clinical databases and electronic data capture (EDC) systems, including case report forms (CRFs). Generate and review Data cleaning listings such as offline listings, medical coding listings and missing pages reports. o Conduct data entry, cleaning, validation checks, and resolve discrepancies to uphold data accuracy, completeness, and compliance with quality standards. Collaborate with cross-functional study teams to resolve data-related issues, integrate feedback, and align data management practices with study protocols. o Adhere to Good Clinical Practice (GCP) and CDISC standards. Note: no travel is required for this role though remote work from "various worksites" permitted. #J-18808-Ljbffr
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