iRhythm Technologies

iRhythm Technologies is a company focused on innovative solutions in the healthcare sector, particularly in the realm of electrocardiogram (ECG) monitoring and analysis. Through the use of advanced technology, iRhythm aims to improve patient care and streamline processes within healthcare environments.

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🔥 Cardiac Technician - California Remote

Posted 2024-11-22

📍 California

🧭 Full-Time

💸 58240 - 70720 USD per year

🔍 Digital healthcare

Experience in ECG/EKG interpretation preferred.
ECG/EKG Technician Certification from an accredited program required.
Associate degree or 2 years college course work preferred; High School Diploma or GED required.
CCT Certification Requirement: You will have 90 days after the conclusion of training to become certified.
Knowledge of medical terminology specific to cardiology is helpful.
Intermediate level PC proficiency.
Excellent interpersonal, organizational, and communication skills.
Excellent attention to detail.
Positive attitude and team player.

Reading, interpreting, and reporting on 90 second ECG strips in a fast-paced environment.
Continuously develop clinical knowledge, particularly ECG rhythm interpretation skills.
Ensure quality reports while meeting productivity metrics.
Communicate critical findings to medical professionals verbally and in writing.

Communication SkillsAttention to detailCoaching

Posted 2024-11-22

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🔥 Sr. Clinical Scientist

Posted 2024-11-07

📍 United States

🧭 Full-Time

💸 146600 - 195000 USD per year

🔍 Digital healthcare

Advanced Degree in Biomedical Science or Health-related field required (MD, PhD preferred).
7+ years of clinical science or clinical development experience in medical device or related industries.
Clinical research experience in heart rhythm disorders, atrial fibrillation, or cardiology.
Experience in observational study design and clinical trial design.
Strong understanding of causal inference.
Working knowledge of diagnostic testing metrics (Sensitivity, Specificity, etc.).
Knowledge of GCP, FDA and EU regulations regarding medical devices.
Experience with clinical trial and observational study design.
Understanding of basic and intermediate biostatistics.
Strong writing skills for clinical documentation.
Ability to collaborate with cross-functional teams.
Experience in program management and project oversight.
Read, write and speak fluent English.
Willingness to travel domestically and internationally (less than 30% work time).

Proactively manage project-level scientific aspects of clinical research projects, including study design, analysis, and evidence dissemination.
Support the Clinical Science function in development of clinical evidence strategies.
Work closely with internal and external stakeholders to ensure robustness of clinical findings.
Lead development of clinical study design and study protocols for prospective trials.
Develop analysis plans and drive analysis and interpretation of clinical data.
Lead evidence dissemination through scientific writing and collaborations.
Support health economics and outcomes research and regulatory teams.
Provide updates on study progress and ensure adherence to standards.

GCPProduct ManagementCollaboration

Posted 2024-11-07

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🔥 Chief Medical Safety Officer; VP, Clinical Oversight & Innovation

Posted 2024-11-07

🧭 Full-Time

💸 287900 - 429200 USD per year

🔍 Digital healthcare

MD or equivalent medical degree with board certification in cardiac electrophysiology or cardiology.
Active medical license.
Minimum 15 years combined experience in clinical practice, academic medicine, and medical device industry.
Strong understanding of FDA regulations and regulated products in cardiovascular disease.
Experience in ambulatory ECG IDTF operations and clinical workflows.
Expertise in AI and machine learning applications in healthcare.
Demonstrated ability to implement medical safety programs and lead clinical innovation.

Ensure comprehensive medical safety governance from product design to post-market surveillance.
Oversee adverse event monitoring and collaborate with Quality and Regulatory Affairs for compliance.
Provide clinical supervision of IDTF services ensuring safety and compliance.
Guide medical expertise throughout the product lifecycle and participate in regulatory submissions.
Support scientific initiatives and represent the company at scientific conferences.

Posted 2024-11-07

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🔥 Software Quality Assurance Engineer II

Posted 2024-10-21

📍 United States

🧭 Full-Time

💸 85400 - 115000 USD per year

🔍 Medical device/software industry

Bachelor’s degree in a technical discipline.
At least 2 years of software testing experience.
Experience as a telemetry/monitor technician or Holter scanner, with ability to interpret ECG records.
Previous experience in testing medical devices and understanding documentation requirements.
Excellent analytical and problem-solving skills.
Self-motivated with ability to work independently and in cross-functional teams.
Effective written and verbal communication skills and attention to detail.
Ability to learn new software tools and concepts quickly.
Strong understanding of QA principles, Design Control procedures, and DHF deliverables.
Knowledge of MySQL and Linux environments with ability to execute SQL queries.
Experience in an agile development environment.

Develop software verification test protocols, test plans, and document test results consistent with compliance requirements.
Review user, system, and software requirements for accuracy and testability, advocating for end-user needs.
Evaluate updates to clinical tools to ensure needs are met for internal and external consumers.
Support new product releases, including preparation of FDA submissions.
Analyze test failures for repeatability and establish regression test scope, working closely with developers.
Participate in agile scrum teams, reporting status in project meetings and supporting DHF activities.

Software DevelopmentSQLAgileMySQLQASCRUMAlgorithmsCommunication SkillsLinux

Posted 2024-10-21

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🔥 Key Account Manager- Michigan

Posted 2024-10-21

📍 US

🧭 Full-Time

💸 85300 - 100000 USD per year

🔍 Healthcare/Medical Devices

Bachelor’s degree is highly preferred or equivalent combination of education, training, and experience.
At least 3 years in an account management or customer success role supporting large or complex accounts.
Proven experience as an Account Manager in healthcare or medical devices.
Self-directed and proactive with strong communication skills.
Ability to multi-task and prioritize in a fast-paced environment.
Proficiency with CRM tools like Salesforce and Microsoft Office.
Exceptional collaboration skills and flexibility.
Willingness to travel up to 20%.

Provide superior support to grow, nurture, and maintain high-volume accounts.
Cultivate long-term customer relationships while meeting and exceeding KPIs.
Proactively deliver value services and advocate for required solutions.
Collaborate with marketing, customer care, and clinical operations teams.
Serve as the primary escalation point for customers.
Drive customer performance by monitoring registration volume and satisfaction.
Train customers on iRhythm service tools.
Evaluate processes to suggest improvements.
Manage and support assigned accounts and attend key customer meetings.

LeadershipBusiness DevelopmentData AnalysisCross-functional Team LeadershipBusiness developmentData analysisCommunication SkillsAnalytical SkillsCollaboration

Posted 2024-10-21

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iRhythm Technologies

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