Leads global implementation team for AI-driven radiology reporting solutions, overseeing deployments, standardization, and client adoption across US, Canada, and Europe. Requires 10+ years in healthcare IT focused on radiology/speech tech and 5+ years leading implementation teams.
Salary not listed
Hybrid10+ YOEOther
About the role
Responsibilities
Lead, develop, and scale a high-performing team of project managers, technical engineers, and implementation consultants supporting Fluency for Imaging and Fluency Direct deployments.
Oversee end-to-end implementation delivery of Fluency for Imaging across the United States, Canada, and Europe, ensuring adherence to scope, budget, and timelines.
Oversee implementation of Fluency Direct across the United States and Canada.
Drive standardization of implementation methodologies, tools, and best practices specific to radiology reporting, dictation workflows, and clinical documentation optimization.
Lead change management and adoption efforts among radiologists, ensuring effective training and long-term utilization of speech recognition and AI capabilities.
Partner with Sales and Solutions teams during pre-sales to support solution design, technical validation, and accurate scoping.
Collaborate with Product and Engineering to incorporate client feedback, regulatory requirements, and workflow enhancements into the product roadmap.
Establish and maintain implementation best practices, methodologies, and delivery frameworks.
Identify and proactively mitigate risks related to system implementation, including user adoption, voice recognition accuracy, and system performance.
Serve as executive sponsor for key customer implementations and manage escalations to successful resolution.
Track, analyze, and report on key performance indicators, including customer satisfaction, team utilization, and project throughput.
Ensure compliance with healthcare regulations, contractual obligations, data privacy standards, and organizational policies.
Drive client satisfaction through strong governance, proactive communication, and disciplined execution.
Requirements
10+ years of experience in healthcare IT, with a focus on radiology, clinical documentation, or speech recognition solutions.
5+ years of leadership experience managing high-performing, high-volume implementation or professional services teams.
Strong understanding of radiology workflows, including dictation, reporting, and results distribution.
Director of Regulatory Affairs and Quality Assurance
EightsleepSan Francisco, CA
Lead risk management, regulatory submissions (FDA 510(k), De Novo), and quality systems (ISO 13485/14971) for medical device sleep technology. Requires 8+ years in medical device QA/RA, successful FDA clearances, and cross-functional leadership with R&D and Clinical teams.
Salary not listed
On-site8+ YOEOther
Director of Medical Operations
EightsleepSan Francisco, CA
Lead medical operations for sleep fitness medical devices at Eight Sleep. Implement manufacturing controls, oversee design verification/validation testing, FDA clearances, and risk management while collaborating with R&D, QA/RA, and clinical teams. Requires 8+ years medical device operations experience and successful FDA track record.
Salary not listed
On-site8+ YOEOther
Director, Investor Relations
AnthropicSan Francisco, CA
Build and lead Anthropic's investor relations program as primary contact for the investment community. Synthesize financial, strategic, and AI developments into clear narratives; advise leadership on investor sentiment while building financial models and relationships.
425k – 600k/yr
Hybrid8+ YOEOther
Director, AI & Business Automation
IllumioSunnyvale, CA
Lead enterprise-wide AI transformation as direct report to the CIO. Define AI strategy, architect Agentic AI and hyper-automation workflows, establish governance, drive business process modernization across functions, and deliver measurable ROI.
227k – 272k/yr
On-site15+ YOEOther
Associate Director, GMP Quality
Formation BioBoston, MA +1
The Associate Director, GMP Quality Assurance ensures compliance for Formation Bio's biologics portfolio by reviewing GMP documents, conducting batch releases, leading investigations, auditing CDMOs, and supporting regulatory inspections. Requires 10+ years GMP QA experience in large-molecule manufacturing, bachelor's in a scientific field, and hands-on quality leadership in a dynamic environment.