Director, Medical Excellence, Electrophysiology

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com

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Job Function:

Medical Affairs Group

Job Sub Function:

Medical Affairs

Job Category:

People Leader

All Job Posting Locations:

Irvine, California, United States of America, Yokneam, Haifa District, Israel

Job Description:

Director, Medical Excellence, Electrophysiology

Johnson & Johnson is currently seeking a Director, Medical Excellence, Electrophysiology located in either Irvine, California or Yoknean, Haifa District, Israel.

About Cardiovascular

Fueled by innovation at the intersection of biology and technology, Johnson & Johnson MedTech is developing the next generation of smarter, less invasive, and more personalized treatments. The Cardiovascular team develops leading solutions across heart recovery, electrophysiology, and stroke, building on a proud heritage of advancing standards of care for patients with stroke, heart failure, and atrial fibrillation.

Position Summary

The Director, Medical Excellence, Electrophysiology will provide scientific, clinical, and Medical Affairs leadership in support of electrophysiology products and complimentary software used in the diagnosis and treatment of cardiac arrhythmias. This role will serve as a strategic scientific partner across Medical Affairs, R&D, Clinical Research, Regulatory Affairs, Quality, Compliance, Marketing, Professional Education, and Commercial teams to ensure medical strategies, evidence generation, scientific communications, claims, training, and product lifecycle activities are clinically meaningful, patient-centered, and compliant.

This leader will help translate clinical evidence and product performance insights into clear scientific evidence for appropriate external communication, and high-quality physician education. The role will also support evidence generation, clinical data interpretation, claims substantiation, risk-benefit assessment, product launch readiness, and lifecycle management across the Electrophysiology portfolio.

Key Responsibilities

The Director, Medical Excellence, Electrophysiology will:

• Provide Medical Affairs leadership and scientific expertise for electrophysiology products, software-enabled technologies, and related clinical workflows across the product lifecycle.
• Partner with R&D, Clinical Research, Regulatory Affairs, Quality, Compliance, Health Economics, Professional Education, Marketing, and Commercial teams to shape integrated medical evidence to support product development, regulatory submissions, claims, launch readiness, training, and post-market evidence needs.
• Lead the medical review and interpretation of clinical, preclinical, real-world, and product performance data to support evidence generation, claims development, physician education, publications, regulatory documentation, and lifecycle management.
• Contribute to evidence generation strategies for company-sponsored studies, investigator-initiated research, registries, post-market studies, and other scientific initiatives aligned to business, clinical, regulatory, and patient-care priorities.
• Provide scientific input and oversight for clinical trial concepts, study design, evidence capture, data analysis, reporting, and dissemination in assigned areas of responsibility.
• Collaborate with Clinical Research, Biostatistics, Regulatory Affairs, and other cross-functional partners to prepare clinical investigation reports, scientific summaries, regulatory responses, publication materials, and evidence packages.
• Review and approve scientific, educational, promotional, reporting, and training materials to ensure accuracy, fair balance, appropriate substantiation, and alignment with applicable regulatory, legal, compliance, and Medical Affairs standards.
• Support scientific communications and publication planning by prioritizing publication concepts, reviewing abstracts and manuscripts, and ensuring data are communicated accurately and responsibly.
• Engage with healthcare professionals, key opinion leaders, professional societies, payers, and providers to understand evolving standards of care, unmet clinical needs, evidence gaps, and opportunities to advance patient-centered innovation.

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