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The Associate Manager, RCM will oversee pre- and post-billing operations and manage a team of RCM Specialists. Responsibilities include developing SOPs and KPIs, monitoring billing workflows, and collaborating with teams to enhance processes. The role requires strong leadership and strategic thinking to optimize operational efficiency and compliance.
The QA Document Control Specialist manages and maintains controlled documents within an electronic document management system to ensure compliance with global regulatory standards. Responsibilities include collaborating with cross-functional teams for document revisions, supporting compliance audits, and training staff on eDMS and document control processes.
The Senior Supplier Quality Assurance Specialist supports quality activities related to Supplier Quality Management in compliance with FDA and ISO regulations. Responsibilities include vendor approval, documentation management, supplier performance monitoring, and leading corrective actions based on supplier audits.
As a Data Operations Analyst, you will extract and analyze data to enhance clinical databases, focusing on patient matching for clinical trials. Your role will involve using SQL and dbt to transform data, creating dashboards for reporting, and ensuring quality through rigorous QA processes. You will collaborate with multiple data sources including EMR databases and improve operational processes.
Seek a director to lead the development of Tempus’ multi-modal molecular data model. Responsibilities include implementing scientific strategies for data usage, designing data models, and managing cross-functional projects. The role bridges scientific research and engineering practices to enhance the healthcare sector with AI-driven insights.
The RWE Data Scientist analyzes Tempus data for real-world evidence studies, developing insights for pharmaceutical partners and overseeing data quality and compliance. Responsibilities include conducting statistical analyses, communicating findings, collaborating across teams, and staying abreast of oncology methodologies and regulations.
The Senior Manager of Quality Assurance oversees issue management processes related to compliance with FDA and ISO regulations. Responsibilities include managing nonconformance and corrective action systems, leading process improvements, collaborating with regulatory teams, and analyzing trends to prevent quality issues.
The Senior Business Intelligence Engineer will manage the design and administration of analytics dashboards, collaborate with stakeholders for data analysis, and develop data governance initiatives. Responsibilities include designing data views, performing root cause analyses, and participating in data projects lifecycle management.
The Sales Operations Associate will support the strategic and operational aspects of Tempus' Life Sciences business. Key responsibilities include analyzing sales data for trends, maintaining sales dashboards, preparing reports for business reviews, and collaborating with teams to enhance sales strategies and operational efficiency.
The Quality Assurance Specialist will oversee the certification processes for Tempus products, collaborate across multiple departments to ensure regulatory compliance, assist in audits, maintain QMS documentation, and provide strategies for process improvements. They will support inspections and audits and manage communication with regulatory bodies.
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