About the role
- 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.
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