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Manage revenue accounting under ASC 606 across clinical diagnostics and data licensing streams. Oversee revenue month-end close, journal entries, deferred revenue, reconciliations, contract reviews, SEC filing schedules, SOX controls, billing integrations, and technical accounting analyses. Partner cross-functionally to automate revenue data processes and lead, mentor, and manage revenue accounting staff.

Lead end-to-end coordination of major IT incidents, run incident bridges, communicate status to stakeholders, drive RCA and post-incident remediation, maintain SOPs/runbooks and dashboards, and identify process improvements and automation opportunities.

As a Senior Product Manager, you will oversee product development for Order Processing, manage the roadmap, and lead cross-functional teams to improve operational efficiency while ensuring alignment with strategic goals.

The Staff Product Designer will drive design solutions for AI-enabled healthcare platform workflows, collaborating with teams to influence business strategy and enhance user experience.

The Business Development Director will establish partnerships with government entities, oversee business development processes, and manage relationships with clients within the healthcare sector.

Lead complex clinical assay development projects from inception to commercialization, managing scope, budget, timelines, and cross-functional teams while ensuring compliance with industry regulations and fostering team development.

The Strategy & Operations Associate will support operational execution in transforming clinical data, managing workflows, reporting, and improving efficiency through AI initiatives.

The Machine Learning Scientist will develop AI frameworks for predictive modeling in oncology, collaborating with teams to enhance drug R&D efforts through advanced machine learning techniques and multimodal data integration.

The Senior Manager for Medical Device Cybersecurity will lead the strategy and execution of cybersecurity initiatives for medical devices, ensuring compliance with FDA guidelines and integrating security into product development processes.

As a Senior Quality Engineer, you will lead verification and validation of medical device systems, conduct risk assessments, and ensure regulatory compliance, particularly in relation to FDA and quality control standards while collaborating with cross-functional teams.