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At iRhythm, we are dedicated, self-motivated, and driven to do the right thing for our patients, clinicians, and coworkers. Our leadership is focused and committed to iRhythm’s employees and the mission of the company. We are better together, embrace change and help one another. We are Thinking Bigger and Moving Faster.
About This Role
The Clinical Science Liaison serves as the primary clinical and scientific contact for healthcare providers, supporting appropriate use of ambulatory cardiac monitoring services while managing conversations around off-label and/or investigational uses. In this role, you will provide customer education, while emphasizing regulatory compliance, and scientific exchange to maintain the integrity of interactions and promote safe, evidence-based practices.
Responsibilities and Duties:
· Scientific and Clinical Expertise: Provide expert knowledge on approved indications for iRhythm’s ambulatory cardiac monitoring systems and services.
· Discuss off-label or investigational use only in response to unsolicited scientific inquiries, ensuring compliance with regulatory and legal standards.
· Customer Engagement on Off-Label or SIUU (Scientific Information on Unapproved Use) Topics:
Respond to unsolicited inquiries regarding off-label use with balanced, evidence-based information. Guide healthcare providers toward peer-reviewed studies, medical literature, or ongoing research to support understanding of off-label applications. Travel for onsite support of off-label use and SIUU training (up to 70%). Avoid proactively promoting off-label or investigational use, adhering strictly to company and regulatory guidelines.· Educate providers regarding the boundaries of evidence-based use and the clinical scenarios supported by current guidelines.
· Serve as a scientific resource to commercial and marketing partners. Participate in sales team training, service updates, presentations, journal clubs, and other approved meetings as appropriate.
· Partner with clinical operations and medical affairs groups and compliantly collaborate with commercial team.
Education and Training:
· Conduct educational sessions on the proper application of cardiac monitoring services for approved indications, including arrhythmia detection and other clinically validated uses.
Support for Regulatory Compliance:
Stay updated on FDA, CMS, HIPAA, and IDTF-specific regulations governing device and service use.\ Ensure that discussions regarding off-label use are handled transparently, following FDA guidelines for scientific exchange.Collaboration and Feedback:
· Partner with internal teams (e.g., clinical, compliance, legal, regulatory, medical affairs) to address gaps in clinical protocols or unmet needs identified during discussions of off-label use.
· Provide customer feedback to inform future studies or expanded indications for monitoring technologies.
Qualifications
· Education: Clinical or scientific degree in health sciences (e.g., RN, APN, PA).
· Credentialing or specialization in cardiology, electrophysiology, or diagnostic sciences is an advantage.
Experience
· 3–5 years in an MSL, clinical liaison, or similar role, particularly in a regulated environment such as diagnostics, biomedical devices and/or experience supporting cardiac monitoring IDTFs (Clinical and/or Commercial support).
· Experience addressing off-label use discussions or working within FDA-compliant frameworks is a significant asset.
Skills
· Familiarity with guidelines on off-label use and other SIUU frameworks.
· Strong relationship-building and communication skills for engaging KOLs, cardiologists, and clinical teams.
Compliance in Customer Engagement: To address off-label use or SIUU
· Solicited Only: Engage only when providers inquire specifically about off-label uses.
· Clear Boundaries: Emphasize the distinction between approved and investigational uses, avoiding promotional language.
· Documentation: Keep detailed records of all inquiries and responses for compliance purposes.
· Data-Driven Discussions: Use peer-reviewed literature and unbiased evidence to support conversations
Value Proposition for Providers
The CSL ensures that healthcare providers:
· Gain a comprehensive understanding of the clinical value of ambulatory monitoring services.
· Have access to the latest data supporting both approved applications of the products and services.
· Feel confident in the safety and effectiveness of the product and service, even when considering innovative or investigational uses.
FLSA Status: Exempt
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Actual compensation may vary depending on job-related factors including knowledge, skills, experience, and work location.
Estimated Pay Range$132,800—$160,000 USD
As a part of our core values, we ensure a diverse and inclusive workforce. We welcome and celebrate people of all backgrounds, experiences, skills, and perspectives. iRhythm Technologies, Inc. is an Equal Opportunity Employer. We will consider for employment all qualified applicants with arrest and conviction records in accordance with all applicable laws.
iRhythm provides reasonable accommodations for qualified individuals with disabilities in job application procedures, including those who may have any difficulty using our online system. If you need such an accommodation, you may contact us at taops@irhythmtech.com
About iRhythm Technologies
iRhythm is a leading digital healthcare company that creates trusted solutions that detect, predict, and prevent disease. Combining wearable biosensors and cloud-based data analytics with powerful proprietary algorithms, iRhythm distills data from millions of heartbeats into clinically actionable information. Through a relentless focus on patient care, iRhythm’s vision is to deliver better data, better insights, and better health for all.
Make iRhythm your path forward. Zio, the heart monitor that changed the game.