Jobs at iRhythm Technologies

Leads complex embedded hardware and firmware development projects from concept through production and commercialization. Owns project planning, schedules, resources, risks, documentation, design-control release plans, and cross-functional execution. Acts as scrum master, facilitates technical discussions, coordinates engineering, quality, regulatory, manufacturing, clinical, and commercial teams, and ensures compliance with company and international standards. Supports production release, project health monitoring, and continuous process improvement for medical device products.

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 full-cycle recruitment for professional, technical, and business-critical roles while advising hiring leaders on workforce planning and talent strategy. Develops sourcing and talent attraction pipelines, uses labor market intelligence and recruiting metrics to guide decisions, ensures recruiting compliance, and improves candidate and hiring leader experiences. Partners with HR, compensation, talent management, and business stakeholders, mentors peers, and supports process improvement and strategic initiatives.

Establish and lead the global People & Culture PMO, including governance, portfolio prioritization, resource capacity planning, risk management, executive reporting, benefits realization, and ROI tracking. The role oversees HR technology, talent, rewards, employee experience, workforce management, AI, compliance, and process improvement initiatives. It also develops project management standards, coaches HR practitioners and sponsors, and partners with the Enterprise PMO and Process Excellence 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%.

Supports medical device product development from concept through commercialization and post-market evaluation. Leads design controls, risk management, verification and validation, design history files, traceability, risk assessments, change evaluations, technical reporting, and audit support. Partners with hardware, firmware, software, and engineering teams to ensure compliance with quality systems, medical device regulations, and standards including IEC 60601, IEC 62366, IEC 62304, ISO 13485, and ISO 14971.

Leads enterprise-wide IT and digital transformation strategy, roadmap development, ERP and business application modernization, enterprise architecture, commercial systems, global invoicing, and post-merger technology integration. Oversees transformation portfolios, budgets, vendors, governance, compliance, and value realization across manufacturing, quality, supply chain, finance, human capital, and commercial operations. Builds high-performing technology teams and partners with executives to deliver measurable operational, financial, and customer experience improvements in a regulated environment.

Analyzes and visualizes post-market surveillance and quality-system data to support complaint handling, investigations, CAPA, regulatory reporting, audits, and inspection readiness. The role prepares reports and regulatory content, applies statistical techniques, identifies product quality trends, and recommends process improvements while partnering with Post-Market Quality and cross-functional stakeholders.

Drive growth for the Zio cardiac monitoring platform across a Raleigh-area territory. Responsibilities include acquiring new healthcare customers, managing the full sales cycle, developing territory plans, presenting clinical and economic value, building relationships with cardiologists and healthcare executives, managing Salesforce pipelines and account health, coordinating onboarding and training, analyzing market performance, and achieving sales goals. The role requires extensive field travel throughout the territory.

Drive growth for iRhythm’s Zio cardiac monitoring platform across a defined territory. Responsibilities include acquiring new business, expanding health-system adoption, managing the full sales cycle, developing strategic relationships with cardiologists and healthcare stakeholders, maintaining Salesforce pipeline accuracy, optimizing account performance, analyzing market activity, and achieving sales targets. The role requires extensive field travel and collaboration with cross-functional teams.

Field-based Territory Manager responsible for acquiring new business and expanding adoption of the Zio cardiac monitoring platform. Manage full sales cycle with cardiologists, electrophysiologists, and health system stakeholders, build pipelines in Salesforce, execute territory growth plans, collaborate cross-functionally, and meet quarterly and annual sales targets. Extensive in-territory travel required.

The Territory Manager will drive growth by acquiring new business and expanding the adoption of the Zio platform among cardiologists and healthcare systems. Responsibilities include developing territory plans, managing accounts, and analyzing market performance.

The Director of Market Access Strategy will develop and execute payer strategies, negotiate contracts, and influence cross-functional outcomes to enhance access and revenue growth in cardiac health solutions.

Lead daily operations of a 20–25 person clinical services team, drive KPIs and performance improvements, manage staffing and budgets, ensure FDA and regulatory compliance, oversee escalation and customer recovery, implement workflow automation and dashboards, coach staff, coordinate training, and contribute to strategic and cross-functional continuous improvement initiatives.

The role involves testing embedded systems software and desktop applications, defining testing strategies, developing protocols, and ensuring quality adherence in regulated environments.

Field-based Territory Manager responsible for driving adoption of the Zio platform across cardiology and EP practices. Own full sales cycle, expand market share, build KOL relationships, manage accounts and pipeline in Salesforce, collaborate cross-functionally, and meet quarterly and annual sales targets while traveling extensively within the territory.

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.

Manage intake, evaluation, investigation, documentation, and closure of product complaints per regulatory requirements. Classify complaints, perform root cause analysis with cross-functional teams, document records in the eQMS, and drive corrective and preventive actions to improve product quality and patient safety.

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.