We anticipate the application window for this opening will close on - 28 Aug 2025

At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll lead with purpose breaking down barriers to innovation in a more connected compassionate world.

A Day in the Life

Together we can change healthcare worldwide. At Medtronic we push the limits of what technology therapies and services can do to help alleviate pain restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be. We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Lets work together to address universal healthcare needs and improve patients lives. Help us shape the future.

At Medtronic we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. This position is remote to enhance our competitive edge and expand our cross-functional collaboration efforts. This role will require 50% - 75% travel to enhance collaboration and ensure successful completion of projects.

Coronary & Renal Denervation therapies are a vital component of the Medtronic Cardiovascular Portfolio. Our team is passionate about the patients we serve around the globe and the second life and improved health we can give to those with Coronary Artery Disease High Blood Pressure and other conditions. Were also driven by the promise of Renal Denervation and its potential to change the way patients around the world manage their uncontrolled hypertension.

Renal Denervation (RDN) is an innovative procedure that helps patients lower blood pressure. The technique targets specific nerves near the kidneys that can become overactive and cause high blood pressure also known as hypertension. High blood pressure is a global epidemic affecting one-third to one-half of adults.

We are seeking a Sr. Field Clinical Research Specialist who will have the responsibility of providing technical and educational support to physicians globally. This is a unique opportunity to be part of a dynamic team that will be responsible for introducing a new therapy that will potentially transform healthcare in the United States. Renal Denervation (RDN) has the potential to be a multibillion-dollar market globally over the next five years. Medtronic is the leader in the RDN field with anticipated FDA approval of our newest device in the next 18 months. Come join the US RDN launch team for a once-in-a-career opportunity to help bring a novel therapy to US Hypertension (HTN) patients.

A Day in the Life

You will be responsible for clinical trial site management case coverage and clinical trial data tracking. This is field based customer facing position. You will be the front line of Medtronic clinical study conduct at the site level forming customer relationships that will ensure studies are conducted effectively and efficiently in accordance with applicable laws and regulations.

Responsibilities:

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

• Provides field support for various clinical research studies by selecting sites performing activation duties setting up protocols providing training helping to enroll participants supporting cases ensuring quality data acquisition and performing study closure activities.

• Addressing clinical research site needs by maintaining frequent contact via email/phone/on-site visits with principal investigators sub-investigators and research coordinators.

• Responsible for gaining and maintaining knowledge of clinical sites in a given geographic area to best understand and assess investigators interests and capabilities.

• Provides continuous communication to in-house clinical trial leaders regarding the status and performance of multiple studies.

• Assist with overall successful conduct of assigned clinical studies consistent with applicable regulations guidelines and policies.

• Interface with representatives from key functional groups (Monitoring Data Management Research & Development Manufacturing Sales Marketing Regulatory Affairs Legal and European Clinical groups).

• Identify and mitigate quality risks and issues for assigned clinical studies with oversight from study management. Oversee follow-up and resolution of site issues.

• Assist in control of device allocation distribution and reconciliation.

• Assist with oversight of activities performed by Contract Research Organizations (e.g. CROs core labs).

• Refer to Standard Operating Procedures (SOPs) and study management process for guidance on everyday study tasks.

• Participate in training to enhance knowledge base.

Must Have:

• Bachelors degree with 4 years of clinical research/clinical (e.g. field clinical research/clinical specialist/field clinical engineer) experience

OR

• Advanced degree with 2 years of clinical research/clinical (e.g. field clinical research/clinical specialist/field clinical engineer) experience

Nice to Have:

• Hospital/clinical experience

• Experience in Good Clinical Practice (GCP) and regulatory compliance guidelines for clinical trials

• Certification from a Clinical Research Association (CCRP/CCRC)

• 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)

• Experience in a Cath lab biomedical engineering hospital/clinic or medical sales

• 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 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.

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. We offer a wide range of benefits resources and competitive compensation plans designed to support you at every career and life stage.

Salary ranges for U.S (excl. PR) locations (USD):$108000.00 - $162000.00

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

The base salary range is applicable across the United States excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience certification/education market conditions and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).

The following benefits and additional compensation are available to those regular employees who work 20 hours per week: Health Dental and vision insuranceHealth Savings AccountHealthcare Flexible Spending AccountLife insurance Long-term disability leaveDependent daycare spending accountTuition assistance/reimbursement andSimple Steps (global well-being program).

The following benefits and additional compensation are available to all regular employees:Incentive plans 401(k) plan plus employer contribution and matchShort-term disabilityPaid time offPaid holidaysEmployee Stock Purchase PlanEmployee Assistance ProgramNon-qualified Retirement Plan Supplement (subject to IRS earning minimums) andCapital Accumulation Plan (available to Vice Presidents and above or subject to IRS earning minimums).

Regular employees are those who are not temporary such as interns. Temporary employees are eligible for paid sick time as required under applicable state law and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.

Further details are available at the link below:

Medtronic benefits and compensation plans

About Medtronic

We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission to alleviate pain restore health and extend life unites a global team of 95000 passionate people.
We are engineers at heart putting ambitious ideas to work to generate real solutions for real people. From the R&D lab to the factory floor to the conference room every one of us experiments creates builds improves and solves. We have the talent diverse perspectives and guts to engineer the extraordinary.

Learn more about our business mission and our commitment to diversity here.

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 addition Medtronic will provide reasonable accommodations for qualified individuals with disabilities.