Senior Clinical Research Specialist - Cardiac Ablation Solutions at Medtronic in Mounds View, Minnesota

Job Description:

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
Site Manager for Cardiac Ablation Solutions
Careers That Change Lives

In this exciting role as a Sr. Clinical Research Specialist, you will have primary focus responsibility to assist with study management duties for assigned clinical programs to evaluate performance, safety, and efficacy of products and to satisfy applicable regulatory standards and Medtronic internal requirements for clinical studies. You will work with the Clinical Management to satisfy applicable regulatory standards and Medtronic internal requirements for clinical studies. Under direct supervision, assumes project management responsibilities for selected studies and site management activities as needed.

The Cardiac Ablation Solutions (CAS) business is one of the fastest growing businesses and helps patients all over the globe requiring mapping and ablation for cardiac arrhythmias. The Cardiac Ablation Solutions Operating Unit focuses on Arrythmia disease management (including Atrial Fibrillation).

Join a diverse team of innovators who bring their worldview, their unique backgrounds, and their individual life experiences to work every day. It's no accident - we work hard to cultivate a workforce that reflects our patients and partners. We believe it's the only way to drive healthcare forward and remain a global leader in medical technology and solutions. To learn more about Inclusion & Diversity at Medtronic Click Here

Primary location is Mounds View, MN; will consider remote position within the United States.

Travel up to 20%.

A Day in the Life

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

• Serves as single point of contact for assigned clinical sites to ensure proper execution of clinical studies in the CAS OU.


• Review patient data to ensure study protocol inclusion/exclusion criteria is met and patient is appropriate candidate for therapy


• Works with assigned sites to ensure adequate subject enrollment that feeds into overall study objectives


• Conducts registered and non-registered clinical studies of products that have been determined to satisfy a medical need and/or offer a commercial potential


• Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), Good Clinical Practice (GCP) and specific country regulations


• Responsible for site nomination and qualification for given sites in assigned territory


• Builds and maintains optimal relationships and effective collaborations with various internal and external parties (i.e., clinical site physicians, nurses, echocardiographers, sonographers, etc.)


• Assists with overall successful conduct of assigned clinical studies consistent with applicable regulations, guidelines, and policies


• Participates in overall clinical management plan, protocol and case report form development


• Provides support and training for clinical study teams, physicians, and cross-functional partners to assure data integrity and protocol compliance. Assists in preparation of study materials and/or training and tracks and maintains study documentation.


• Performs data review, reviews data discrepancies, generates reports and works with sites for timely discrepancy resolution


• May interface with representatives from key functional groups including Product Development, Therapy Development, Manufacturing, Sales & Marketing, Distribution, and Regulatory Affairs


• Assists clinical management with other duties as requested

Must Have (Minimum Requirements):

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

• Bachelor's degree


• Minimum of 4 years of clinical research experience OR


• Advanced degree with 2 years of clinical research experience

Nice to Have (Preferred Qualifications):

• Degree in life sciences, or related medical/scientific field.


• Experience conducting/working on clinical studies and managing clinical trial data review


• Clinical Research experience at Medtronic or within a medical device industry, preferably in cardiovascular area


• CCRA certification (Certified Clinical Research Association) or SOCRA.


• Strong knowledge of clinical monitoring functions and clinical research methodologies, including study design, implementation, and reporting.


• Experience with Clinical Operations and interfacing with CRO teams.


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


• Excellent project management and organization skills.

About Medtronic
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. Let's work together to address universal healthcare needs and improve patients' lives. Help us shape the future.

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. (ADA-United States of America)

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.

Learn more about our benefits at benefits.medtronic.com

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):$105,600.00 - $158,400.00

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).

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 90,000+ 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 law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.

At Medtronic, most positions are posted on our career site for 3-7 days.