An experienced cardiac electrophysiologist will provide medical leadership for electrophysiology and left atrial appendage closure therapies across the product lifecycle, with a focus on clinical evidence, benefit-risk assessment, and patient safety. The role supports product development, clinical studies, post-market surveillance, and scientific review, while also serving as the clinical voice in cross-functional decision-making. This is a hybrid physician leadership position that works closely with research, quality, regulatory, R&D, marketing, and business development teams.
Key Responsibilities
- Serve as a medical expert and patient advocate across electrophysiology and LAAC therapies.
- Provide medical leadership and benefit-risk assessment for product development, clinical studies, and post-market activities.
- Provide medical oversight for clinical trials, including protocol development, investigator engagement, safety monitoring, data interpretation, and dissemination of findings.
- Support post-market surveillance, including safety signal evaluation, device performance assessment, and health risk analysis.
- Collaborate with internal teams and external health care providers to review adverse events and emerging clinical concerns.
- Review and approve clinical, scientific, and regulatory documents, including evidence reports, safety communications, and risk management materials.
- Provide medical review of scientific, educational, and promotional content for clinical accuracy and compliance.
- Support training, mentorship, and development of medical and cross-functional teams.
Required
- Valid and unrestricted MD degree or accepted international equivalent.
- Board certified or board eligible in Clinical Cardiac Electrophysiology, or equivalent international certification.
- Valid, unrestricted medical license in good standing.
- At least 5 years of experience as an independent cardiac electrophysiologist.
- Experience managing complex arrhythmias and performing advanced electrophysiology procedures.
- Working knowledge of clinical trial design, Good Clinical Practice, and medical device development.
Preferred
- Experience as a clinical investigator or on an IRB, Clinical Events Committee, or similar oversight body.
- Knowledge of global medical device regulations, post-market surveillance, and medical safety practices.
- Experience supporting innovation, business development, or technology assessment activities.
- Familiarity with electrophysiology practice across diverse health care systems.
Benefits & Perks
- Hybrid work model.
- Opportunity to work with a global medical technology leader.
- Access to tools, information, and training to support skill and career development.
- Salary range provided for the role.
- Potential annual bonus and long-term incentives for exempt roles, subject to eligibility.