Senior Clinical Research Specialist - CAS remote type Remote locations Mounds View, Minnesota, United States of America time type Full time job requisition id R60621 We anticipate the application window for this opening will close on - 1 Jul 2026 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 Cardiac Ablation Solutions (CAS) offers cardiac mapping and ablation solutions to treat patients with abnormal heart rhythms. Our vision is to help patients worldwide by advancing innovation for the diagnosis and ablation of cardiac arrhythmias, enabling clinicians to perform procedures with superior outcomes. 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 25% of travel to enhance collaboration and ensure successful completion of projects. In this exciting role as the Senior Clinical Research Specialist (CRS) within the CAS Operating Unit, you will be responsible for driving and overseeing execution of key clinical programs to support the development and advancement of best-in-class ablation therapies.  The Senior CRS is responsible for developing strategies and driving processes to meet the milestones of complex clinical studies/projects in compliance with applicable clinical and regulatory standards and in alignment with Medtronic business needs. The Senior CRS sets work direction for the study team and owns the study data to ensure that all data collected is comprehensive, accurate, and up to date. The Senior Clinical Research Specialist will collaborate with other members of the CAS leadership team, as well as other cross-functional stakeholders (e.g., Research and Development, Corporate Biostats, Regulatory Affairs, Clinical IT, and others). In this role, you will collaborates, build relationships, and communicates effectively with a large group of internal and external stakeholders in a rapidly changing landscape, while managing the timely completion of deliverables. This role has a high-level of visibility to senior leaders at Medtronic including Executive Committee members and senior clinical leaders across all OUs. 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. For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required. 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. U.S. Work Authorization & Sponsorship At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment. Join us in our mission to alleviate pain, restore health, and extend life—where your unique background and perspective are valued. 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). The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple 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 match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital 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 95,000+ 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. If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

• Provide high-quality nursing care to clinical trial participants in their homes • Perform study-related procedures, including but not limited to: - Vital signs - Specimen collection, processing, and shipment - Electrocardiograms (ECGs) - Process specimens and ship specimens per protocol. • Administer investigational medications/products per study protocol • Conduct patient assessments and monitor for adverse events; report findings to the study team/Principal Investigator • Accurately document all visit activities in accordance with study requirements • Educate patients on study procedures, medications, and compliance • Maintain adherence to ICH-GCP guidelines and study protocols • Communicate effectively with patients, caregivers, and study teams • Maintain strict adherence to HIPAA and all applicable patient privacy regulations, ensuring secure handling and confidentiality of protected health information (PHI)

• Provide high-quality nursing care to clinical trial participants in their homes • Perform study-related procedures, including but not limited to: - Vital signs - Specimen collection, processing, and shipment - Electrocardiograms (ECGs) - Administer investigational medications/products per study protocol • Conduct patient assessments and monitor for adverse events; report findings to the study team/Principal Investigator • Accurately document all visit activities in accordance with study requirements • Educate patients on study procedures, medications, and compliance • Maintain adherence to ICH-GCP guidelines and study protocols

Role Description In this role, you'll be accountable for making decisions that directly impact our members while managing a demanding case load in a rapidly-changing, production-driven environment. - Perform clinical coverage review services, which require interpretation of state and federal mandates, applicable benefit language, and consideration of relevant clinical information. - Communicate all types of benefit determinations, including decisions regarding coverage guidelines, contractual limitations, and reimbursement determinations. - Speak with health care providers and/or members to explain benefit coverage determinations and obtain additional clinical information. Qualifications - Associate's degree - Current unrestricted RN license in the state of Massachusetts - 3+ years of experience as a RN, including experience in an inpatient/acute setting - 1+ years of clinical documentation experience - A designated homework space with access to install secure high-speed internet via cable/DSL Requirements - A background in utilization review for an insurance company or experience in case management (preferred) - Familiarity with Milliman Care Guidelines (preferred) - Critical thinking skills (soft skill) Benefits - Comprehensive benefits package - Incentive and recognition programs - Equity stock purchase - 401k contribution (all benefits are subject to eligibility requirements) - Hourly pay range: $29.00 to $52.00 per hour based on full-time employment