Jobs at iRhythm Technologies

Supports clinical and observational study design, statistical analysis, documentation, and reporting for cardiology medical devices. Develops and validates SAS programs, creates statistical analysis plans, performs quality control of datasets and TLFs, supports FDA remediation and regulatory submissions, and communicates findings to cross-functional stakeholders. Requires advanced SAS programming and knowledge of clinical trial data, CDISC standards, and statistical methods.

Drives growth for iRhythm’s Zio cardiac monitoring platform across a defined territory. Responsibilities include acquiring new business, expanding healthcare-system adoption, managing the full sales cycle, building physician and executive relationships, developing territory plans, maintaining Salesforce pipeline forecasts, optimizing account performance, analyzing market trends, and meeting sales goals. The role requires extensive field travel and collaboration with clinical, payer, billing, customer success, and marketing teams.

Field-based Territory Manager responsible for expanding adoption of iRhythm’s Zio cardiac monitoring platform across South Connecticut. Duties include acquiring new healthcare accounts, managing the full sales cycle, developing territory growth plans, engaging cardiologists and health system stakeholders, managing pipelines in Salesforce, optimizing account performance, analyzing market trends, and meeting sales targets. Requires extensive territory travel and experience in medical device or healthcare technology sales.

The Territory Manager will drive adoption and revenue growth for iRhythm’s Zio cardiac monitoring platform across a defined territory. Responsibilities include acquiring new business, developing strategic sales plans, managing the full sales cycle, engaging cardiologists and healthcare executives, expanding health-system accounts, maintaining Salesforce pipeline data, supporting onboarding and account performance, analyzing market trends, and meeting sales targets. The role requires extensive field travel and collaboration with cross-functional teams.

Leads product discovery, roadmap prioritization, requirements definition, and delivery for clinician-facing digital workflow software. Partners with engineering, design, clinical, regulatory, operations, and commercial teams to launch scalable features, measure adoption and operational impact, and guide post-launch improvements. The role requires healthcare technology experience, strong stakeholder leadership, workflow and systems analysis, analytics proficiency, and familiarity with regulated software, integrations, and product management tools. Remote within the US, with travel up to 20%.

Manage and continuously improve medical-device design control processes across R&D and product development. Translate FDA, ISO, and IEC requirements into practical procedures, SOPs, templates, and implementation plans. Maintain audit-ready Design History Files and traceability, lead risk-management activities, support quality assurance and regulatory compliance, and identify process improvements. Partner with Quality, Regulatory, Manufacturing, and Engineering teams to resolve gaps, influence adoption, and embed consistent design assurance practices throughout the product lifecycle.

Lead execution and architecture for early-stage medtech innovations across AI, sensors, digital biomarkers, and wearables. Drive needs-finding, feasibility, business cases, partnerships, and transition of validated concepts into funded product development while aligning cross-functional stakeholders and managing portfolio timelines, budgets, and evidence strategies.

Lead scientific aspects of clinical research projects including study design, analysis, protocol development, evidence dissemination, and cross-functional collaboration to support device market clearance and post-market evidence. Drive analyses of prospective and real-world data, author regulatory and scientific documents, support HEOR and regulatory teams, and oversee project execution and quality standards.

Lead functional design and implementation of Salesforce CRM (Sales, Service, Life Sciences Cloud). Translate business strategy into scalable, compliant solutions, lead cross-functional requirements gathering, produce functional and technical documentation, guide integrations and data strategy, and partner with product teams and vendors to deliver large-scale Life Sciences programs.

Administer and maintain IRIS for Health integration platforms on AWS EC2 and Linux, manage network security and PaloAlto VPNs, build CI/CD with CodeFresh/GitLab, integrate and troubleshoot EHR interfaces (Epic, Cerner, Allscripts), automate provisioning with scripting (Python, ObjectScript, Bash, JavaScript), implement infrastructure automation, monitor systems, participate in on-call support, and optimize performance and reliability.

Lead global regulatory strategy and submissions for AI-enabled wearable medical devices. Prepare filings, interact with agencies, guide cross-functional teams, maintain registrations, approve design changes, and support labeling, SOPs, and recalls.

Lead QA across multiple concurrent software projects for a regulated medical device platform. Define test strategy, estimation, execution, risk management, and release readiness. Drive automation for API, integration, and backend testing, build CI/CD pipelines, coordinate cross-functional planning, and ensure verification and documentation meet regulatory and quality standards.

Manage and grow iRhythm's largest accounts by building relationships, monitoring KPIs, resolving escalations, training customers on service tools, coordinating cross-functional teams, and driving account performance and workflow efficiencies. Travel up to 20%.

The Principal Software Architect defines and governs software architecture for medical and non-medical systems, ensuring reliability, scalability, and regulatory compliance across multiple platforms, while collaborating with various teams to drive architectural excellence.

Lead and manage a software engineering team building full-stack mobile applications and backend services for a regulated medical device. Provide technical and architectural guidance, collaborate cross-functionally, ensure software quality, compliance, deployments, and support production incident response and corrective actions.

Designs, builds, and supports corporate networks, servers, storage, telephony, and cloud systems across on-prem, colo, and cloud. Leads infrastructure projects, provides technical escalation, mentors staff, manages vendors, drives vulnerability remediation and lifecycle tasks, and supports global 24x7 operations with SOX compliance.

Lead technical ownership of the Gateway Android app for a safety-critical mobile cardiac telemetry product. Architect and implement reliable long-running Android applications, make architectural decisions, write production code, drive design discussions and code reviews, mentor engineers, and establish durable engineering practices. Collaborate with cross-functional teams and ensure robust BLE, background execution, and secure communication capabilities.