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The Senior Data Standards Analyst acts as a metadata expert in the Clinical Information Governance team, providing guidance on clinical data standards and leading governance initiatives for CDISC models. This role involves monitoring regulatory requirements, supporting clinical teams with study-specific metadata, and promoting best practices in data management across global studies.
As a Senior Data Integration Analyst, you will integrate data from clinical trials, implement data flows, and ensure compliance with regulations. Your role involves working with various stakeholders to enhance data reliability and accuracy while supporting continuous improvement in clinical data management processes.
The Signal Manager is responsible for executing risk-based monitoring strategies, overseeing key risk indicators and data quality assessments, and implementing corrective actions to ensure data integrity and patient safety in clinical trials. The role also involves coordinating monitoring activities and escalating issues to stakeholders.
As the Principal Data Integration Analyst, you will oversee data integration for clinical trials, ensuring high-quality data delivery and compliance with regulatory standards. Responsibilities include coordinating with internal and external stakeholders, resolving data integration issues, and leading continuous improvement initiatives. Strong experience in clinical data management and digital tools is essential.
As a Senior Data Integration Analyst, you'll integrate data from clinical trials, implement data flows and mapping according to standards, ensure compliance with GCP and regulations, and resolve data issues while supporting improvements and technical strategies.
The Data Standards Analyst contributes to the development and governance of clinical data standards, supports clinical teams with metadata review, and monitors regulatory requirements. They help in bridging global metadata strategies and therapeutic area studies, as well as assist in developing CDISC-compliant metadata specifications.
The Data Management Programmer will develop programs for data validation and review, support study teams with data management programming, and ensure compliance with project milestones regarding data cleaning. Key responsibilities include developing analytics tools, automating protocol deviations, and optimizing reporting tools.
The role involves providing master data management (MDM) activities, ensuring compliance with standardized processes, performing regular data consistency checks across systems, executing quality control, and participating in continuous improvement initiatives within the finance department.
The Digital Project Lead will oversee high-priority IT projects from initiation to closure, aligning IT initiatives with business strategy. Responsibilities include developing project plans, leading teams, managing stakeholder expectations, and ensuring project success within budget and timelines.
As a Principal Biostatistician, you will support clinical study design, develop statistical sections in protocols, ensure statistical integrity in reports, perform data analysis, and facilitate collaboration within teams and with senior leadership, contributing to vaccine research.
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