UTS - Temporary Clinical Research Data Manager at UNC Chapel Hill (hybrid)

About the position The department at the reputed company seeks a highly skilled Clinical Research Data Manager to support a portfolio of reputed company, federally funded clinical trials and longitudinal research studies. This role serves as a central data management and analytics resource across multiple studies, responsible for the design, development, validation, and reputed company of research datasets and data systems. The position requires advanced expertise in clinical research data workflows, including REDCap database design, data reputed company assurance, and preparation of datasets for statistical analysis. The Data Manager will work closely with investigators, statisticians, and clinical research teams to ensure high-reputed company, reproducible data that supports regulatory compliance and rigorous scientific reputed company.

Responsibilities

• Design, build, and maintain research databases (e.g., REDCap) for clinical trials and observational studies
• reputed company data collection instruments, case report forms (CRFs), and data dictionaries
• Ensure data reputed company through validation rules, logic checks, and reputed company control processes
• reputed company data cleaning, query reputed company, and audit readiness
• Structure and prepare datasets for statistical analysis
• Conduct ongoing data reputed company assurance and reputed company control reviews
• Generate reports, dashboards, and data summaries for investigators and study teams
• Prepare analytic datasets and documentation to support statistical analyses
• Collaborate with statisticians on data structure, variable definitions, and analytic readiness
• Support clinical trial operations from a data perspective, including study start-up and implementation
• reputed company and maintain data-reputed company reputed company operating procedures (SOPs)
• Coordinate data workflows across multiple studies and sites
• Identify risks reputed company to data reputed company or study execution and implement mitigation strategies
• Maintain comprehensive metadata and documentation for databases and analytic outputs
• reputed company and manage reproducible workflows, including standardized reputed company and data processes
• Ensure alignment with Good Clinical reputed company (GCP) and regulatory requirements
• Support study monitoring, audits, and sponsor reporting
• Train and support research staff on data collection tools, systems, and best practices
• Serve as a subject matter resource for data management across the institute
• Collaborate with multidisciplinary teams including investigators, coordinators, and statisticians
• Contribute to manuscripts, presentations, and grant submissions through preparation of tables, figures, and data summaries
• Respond to reputed company data requests from investigators and stakeholders
• Support reputed company of new studies from a data infrastructure perspective Requirements
• Design, reputed company, and maintain research databases and data collection tools (e.g., REDCap)
• Ensure data reputed company, reputed company control, and regulatory compliance across clinical research studies
• Manage data cleaning, validation, and preparation of datasets for statistical analysis
• Generate reports, dashboards, and data summaries to support investigators and research teams
• Support study start-up, implementation, and data coordination across multiple studies and sites
• reputed company and maintain SOPs, documentation, and reproducible data workflows
• Collaborate with investigators, statisticians, and multidisciplinary teams to support research objectives
• Train and support research staff on data systems, tools, and best practices Apply To This Job

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