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The Account Manager will expand collaborations with pharmaceutical partners, oversee the execution of deliverables for clients, manage studies from start to closure, assist in creating processes to accelerate clinical trials, and collaborate across teams to deliver key outcomes while maintaining customer satisfaction.
The RCM Specialist will manage healthcare denials, appeals, and refunds, optimizing revenue cycle operations. Responsibilities include monitoring billing systems, ensuring timely appeals, analyzing denial trends, and collaborating with various departments to enhance revenue cycle management KPIs.
The RCM Specialist I will manage patient billing worklists, troubleshoot patient demographic issues, review clinical documents for claims submissions, update patient information, and analyze workflows for process improvements in Tempus' Internal Billing Operations team.
The Patient Billing & Outreach Specialist manages patient billing processes and conducts outreach to help patients understand their financial responsibilities. Responsibilities include communicating with patients about billing, coordinating with financial assistance teams, ensuring compliance with billing practices, and participating in team meetings for process improvements.
The RCM Specialist I will support accurate coding and billing processes for medical procedures, ensuring compliance with regulations. Responsibilities include coding for molecular oncology testing, managing patient billing worklists, resolving coding issues, and analyzing workflows for efficiency improvements.
The Biostatistician II will lead independent data analyses to support Medical Affairs, focusing on oncology and molecular data. Responsibilities include presenting insights, collaborating with research teams, and staying updated on methodological advancements. Previous experience in computational biology, data science, and utilizing statistical tools is required in this role.
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 Director of Alliance Management is tasked with building partnerships with pharmaceutical companies to enhance their research using Tempus products. Responsibilities include managing data operations, providing scientific support, improving client satisfaction, and addressing partners' needs by developing customized proposals and cross-functional collaboration.
The Senior Supplier Quality Assurance Specialist will support quality activities related to Supplier Quality Management, ensuring compliance with FDA QSR and ISO 13485. Responsibilities include vendor approval, managing documentation, handling corrective actions, monitoring supplier performance, and maintaining supplier metrics.
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.
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