Job Description

Job Opportunity At Abbott

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to:

• Career development with an international company where you can grow the career you dream of.
• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
• An excellent retirement savings plan with high employer contribution
• Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree
• A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
• A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity:

You will provide strategic and operational support to the Chief Medical Officer and the broader Cardiac Rhythm Management (CRM) business. This role is essential to expanding the bandwidth of Medical Affairs and will contribute to product development, clinical trial planning and execution, regulatory support, quality oversight, and external engagement with key opinion leaders and professional societies.

What You'll Work On:

• Lead medical affairs activities for the core technology products (transvenous pacemaker (low voltage), transvenous ICD (high voltage), CRT, ICM(ILR), and Merlin.net.
• Collaborate with R&D on pipeline development and defining new product features.
• Plan and execute clinical studies (IDE, indication expansion, post-approval registries, real-world evidence).
• Draft and review scientific publications.
• Provide medical input for regulatory submissions and health reimbursement strategies globally.
• Support commercial and marketing initiatives with medical expertise.
• Monitor product quality, review risk management reports (RMRs), health hazard evaluations (HHEs), and assist in field action execution.
• Develop and maintain relationships with professional societies, academic medical institutions, and key opinion leaders to advance scientific collaboration and enhance the visibility of CRM initiatives.
• Serve as medical representative on risk evaluation and investigation teams.
• Provide initial medical input for customer communications, technical bulletins, and quality directives.
• Update medical affairs procedural documents and manage change requests.

Qualifications:

• M.D. or D.O. with board certification in Clinical Cardiac Electrophysiology or international equivalent
• 10+ years of clinical practice with deep expertise in cardiac rhythm management, including CIED implantation and follow-up
• Comprehensive understanding of electrophysiology, device-based therapies, and cardiac rhythm interventions.
• Proven experience in medical monitoring, adverse event reporting, and leadership of clinical events committees.
• Skilled in authoring and reviewing promotional, educational, and scientific materials.
• Capable of evaluating product complaints and contributing to safety assessments and surveillance activities.
• Exceptional communication, leadership, and multitasking abilities in fast-paced, cross-functional environments.

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