We anticipate the application window for this opening will close on - 22 Sep 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.

MUST HAVE (MINIMUM REQUIREMENTS):

To be considered for this role, the minimum requirements must be evident on your resume.

• Bachelor’s degree and 2 years of experience in clinical research or as a clinical specialist/field clinical engineer/clinical sales rep
• Or advanced degree and 0 years of experience in clinical research or as a clinical specialist/field clinical engineer/clinical sales rep

NICE TO HAVE (PREFERRED QUALIFICATIONS):

• 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
• Provides technical support to clinical study sites by serving as the technical resource between engineering and the medical community.
• This position is applicable when complex products are involved in clinical trials.
• Typically present during initial implant to determine how the product interacts with a human body.
• Responsible for identifying investigators, presenting protocols for a study, assisting investigators in product application, and submitting status reports on all programs.
• Support research and development in evaluating concepts of new products and modifying existing devices or therapies.
• Individuals in this role are often publishing data and findings in journals and may have existing patents and/or patent applications.

PHYSICAL JOB REQUIREMENTS

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
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. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.

Responsibilities may include the following and other duties may be assigned.

• Provides technical assistance to clinical study sites by serving as the technical resource between engineering and the medical community.
• This position is applicable when complex products are involved in clinical trials.
• 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.
• Individuals in this role are often publishing data and findings in journals and may have existing patents and/or patent applications

Other Responsibilities:

• 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

To be considered for this role, the minimum requirements must be evident on your resume.

• Bachelor’s degree and 2 years of experience in clinical research or as a clinical specialist/field clinical engineer/clinical sales rep
• Or advanced degree and 0 years of experience in clinical research or as a clinical specialist/field clinical engineer/clinical sales re