Job Title: Clinical Fellow – Cardiac Rhythm Technologies
Location: United States – Sylmar, California
Category: Medical & Clinical Affairs
Employment Type: Full-Time
Experience Required: Minimum 12 Years (Electrophysiology / Cardiac Rhythm Management Preferred)
Abbott is a global healthcare leader committed to advancing medical science and improving patient outcomes worldwide. Within Abbott’s Cardiac Rhythm Technologies (CRT) division, we are seeking a highly experienced Clinical Fellow to support next-generation innovation in leadless pacing and conduction system pacing technologies.
This role plays a pivotal part in providing clinical leadership and strategic direction for research and development programs across transvenous and leadless cardiac device portfolios. The Clinical Fellow will work closely with R&D, regulatory, and global clinical teams to generate robust clinical evidence and deliver customer-centric solutions that shape the future of cardiac arrhythmia management.
Lead the development and execution of pre-clinical and clinical feasibility strategies for innovative cardiac device prototypes.
Support research and technology (R&T) and R&D programs through study planning, execution, data collection, statistical analysis, and scientific publication.
Drive clinical evidence generation initiatives that influence clinical practice and support regulatory and commercialization strategies.
Provide clinical expertise in the design and development of next-generation leadless and conduction system pacing technologies.
Collaborate with engineering, quality, and regulatory teams to ensure clinical relevance and compliance across device development lifecycles.
Lead global engagement with key opinion leaders to identify unmet clinical needs, gather product feedback, and support iterative prototype testing.
Support scientific communications, advisory boards, and peer-reviewed publications in collaboration with external clinical experts.
Coordinate with internal stakeholders to deliver high-quality clinical and testing documentation for regulatory submissions.
Ensure alignment with medical device quality systems, global regulatory standards, and internal governance requirements.
MD or PhD with strong cardiovascular, electrophysiology, or cardiac rhythm management expertise.
Deep working knowledge of medical device quality systems, regulatory standards, and clinical research methodologies.
12+ years of experience in electrophysiology (EP), cardiac rhythm management (CRM), or cardiovascular medical device industry roles.
Proven experience supporting clinical research, feasibility studies, and regulatory submissions for implantable cardiac devices.
Contribute to life-changing innovations in cardiac rhythm management and advanced pacing technologies.
Work within a globally recognized organization at the forefront of medical device innovation.
Competitive compensation, comprehensive benefits, and long-term career growth opportunities.
Collaborate with world-class scientists, clinicians, and engineers shaping the future of cardiovascular care.
Compensation Range: USD 172,000 – 344,000 annually (location-dependent)
Gujarat :
Ahmedabad | Ankleshwar | Baroda | Bharuch | Gandhinagar | Gujarat | Halol | Jhagadia | Mehsana | surat | Tarasadi | Vadodara | Vapi |Maharashtra :
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Siliguri |Illinois :
Abbott Park | Bloomingdale | Champaign | Chicago | Deerfield | Glenview | Lake Forest | Lombard | Naperville | Norridge | Park RIdge | Round Lake |Maryland :
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