Job Description

We anticipate the application window for this opening will close on - 17 Oct 2025 At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life In this exciting role as the Senior Field Clinical Engineer (Sr. FCE) for the Cardiac Rhythm Management Operating Unit, you will be responsible for the introduction, implementation and follow-up and closure of clinical studies; support of research and development in evaluating concepts for new products the modification of existing devices; serving as a technical resource between engineering, clinical research, and the medical community. Among these responsibilities, the highest priority is given to the support of clinical studies. Our Cardiac Rhythm Management Integrated Operating Unit offers devices and therapies that treat patients with abnormal heart rhythms and heart failure. It is comprised of three key businesses: Cardiac Pacing Therapies, Defibrillation Solutions, Cardiovascular Diagnostic & Services. Together, we will transform the lives of people with cardiac arrhythmias and heart failure. We are seeking a committed professional to join our team. While this is a remote position not located at a physical Medtronic site, the candidate hired will be required to reside within the territory and drive to multiple accounts throughout the region. A valid driver's license is essential for this role. The territory for this role can either be Wisconsin or Chicago, IL Responsibilities Provides technical assistance to clinical study sites by serving as the technical resource between engineering and the medical community. Typically present during initial implant to determine how the product interacts with a human body. Accountable for identifying investigators, presenting protocols for a study, assisting investigators in product application, and submitting status reports on all programs. Assist research and development in evaluating concepts of new products and modifying existing devices or therapies. Provides all aspects of assistance for Clinical Research studies by identifying investigators, nominating sites, performing activation duties, providing training, encouraging enrollment, ensuring quality data acquisition and performing study closure activities. Accountable for gaining and maintaining knowledge of clinical sites to best understand and assess physicians’ interests and capabilities. Develops expertise in clinical and market released products and functions as a local technical/clinical resource for Medtronic and the customer. May be present in the operating room during clinical procedures as well as physician office to facilitate patient testing and data collection. Accountable for developing and leveraging relationships in the field to drive clinical activity and maintain focus on the customer. Provides feedback from clinical sites on the performance of the product to be incorporated in engineering designs or enhancements, Assists research and development in evaluating concepts for new products, and considers potential modifications for existing devices while serving as a technical resource between engineering and the medical pacing community. Provides prospective and real-time feedback to clinical study management in study design and document development. Plays a critical role in educating customers, sales partners and internal Clinical Research talent on the technology that they assist. Required Knowledge and Experience: Requires a Baccalaureate degree Minimum of 4 years of experience in clinical research or as a clinical specialist/field clinical engineer/clinical sales rep Or Masters degree and 2 years of experience in clinical research or as a clinical specialist/field clinical engineer/clinical sales rep. Or Phd with 0 Years of experience Nice to Have (Preferred Qualifications): 2 years experience at Medtronic or within the medical device industry Experience in the management of clinical devices. Cardiovascular/Cardiac rhythm management device training (e.g., pacemakers & defibrillators) strongly preferred. Experience in a Cath lab, biomedical engineering, hospital/clinic or medical sales. Experience in Good Clinical Practice (GCP) and/or regulatory compliance guidelines for clinical trials. Experience in clinical studies and/or trial site management/protocols. Experience collaborating with cross functional clinical partners/customers, physicians and/or medical sales colleagues in the healthcare industry Physical Job Requirements The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Benefits & Compensation Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. Salary ranges for U.S (excl. PR) locations (USD): $104,000.00 - $156,000.00 Equal Employment Opportunity It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. #J-18808-Ljbffr Medtronic

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