Clinical Research Spec

Medtronic; Mounds View (MN); On-site; USD 83,000 - 125,000; Full time

Benefits offered by this job

Health, Dental and Vision Insurance

401(k) with employer match

Tuition assistance

Job summary

Medtronic's ICT Clinical Research Specialist in Mounds View, MN, leads study execution and site management for key device-based technologies. You will work with the Clinical Study Manager to meet regulatory standards and internal requirements while supporting site training and data integrity.

The role emphasizes cross-functional collaboration, adherence to GCP, and proactive site issue resolution across global teams. In-person work is required to drive the study program forward.

Qualifications

• Bachelor's degree and minimum of 2 years of clinical research experience.
• Certification such as CCRA/SOCRA is preferred.
• Experience managing multiple clinical research sites and ensuring protocol compliance.

Responsibilities

• Review and approve required documents for study start and ongoing validity.
• Perform site initiation, issue resolution, and study closure activities.
• Provide training and support for clinical study sites to ensure data integrity and protocol adherence.
• Set up and maintain accurate clinical study files and site coordination.
• Oversee operational aspects of trials with SOP, GCP, and country regulations.

Skills

Clinical research

Site management

Regulatory compliance

Data review

Education

Bachelor's degree

Advanced degree

Job description

We anticipate the application window for this opening will close on - 13 Oct 2026Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.A Day in the LifeThe ICT portfolio delivers differentiated cardiovascular technologies that help clinicians detect and manage cardiac conditions earlier, treat patients more effectively, and improve outcomes. By combining advanced device innovation, actionable data, and connected care capabilities, the portfolio supports better clinical decision-making and creates value for patients, providers, and healthcare systems.At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We’re working a minimum of 4 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.This position will be based in Mounds View, MN.In this exciting role as a Clinical Research Specialist within the Interventional Cardiology Therapies (ICT) Operating Unit, you will have primary focus and responsibility for study execution and clinical study site management on a key clinical program to support the development and advancement of best-in-class ICT device-based technologies. You will work under the direction and closely with the Clinical Study Manager to satisfy applicable regulatory standards and Medtronic internal requirements for clinical studies.Reviews and approves required documents for study start, assures continued validity of such documents, takes actions for updates and/or replacements, and monitors site activationPerforms site initiation activities, resolution and follow-up of site issues, and study closure activities.Provides support and training for clinical study sites to assure data integrity and protocol compliance.Prepares study materials and/or training and tracks and maintains study documentation.Sets up and maintains accurate clinical study files.Coordinates activities of associates (assigned clinical site staff) and investigators to ensure compliance with CIP and overall clinical objectivesPerform site file reviewsOversees 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 and may prepare clinical trial budgets.Participates in overall clinical management plan, protocol and case report form development.Performs data review, reviews data discrepancies, ensures data queries are being resolved, works closely with monitors to ensure monitoring action items are resolved, and generates reports.Reports on progress and results of clinical investigationsMay be responsible for clinical supply operations, site and vendor selection.Builds and maintains optimal relationships and effective collaborations with various internal and external parties.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 and a minimum of 2 years of clinical research experienceOr advanced degree with 0 years of experienceNice to Have (Preferred Qualifications):Degree in engineering, life sciences, or related medical/scientific fieldCCRA certification (Certified Clinical Research Association), SOCRAClinical research/clinical trials experience at Medtronic or within the medical device industryExperience in Good Clinical Practice (GCP) and/or regulatory compliance guidelines for clinical trialsExperience managing multiple clinical research sites with proven results in study executionExperience in clinical operationsExperience developing clinical strategies and study designExperience working on a global study teamExperience in Research and Development (R&D)Project/program management skills/experienceAbility to appropriately apply different standards related to medical devices/clinical research (SOPs, GCP, ISO, ICH, FDA, MEDDEV, MDR, etc.) as neededFor 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 RequirementsThe 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 & SponsorshipAt 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.Recruitment Fraud AlertWe are aware of phishing scams targeting job seekers. Please keep the following in mind:Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at [e-mail] .Benefits & CompensationMedtronic offers a competitive Salary and flexible Benefits PackageA 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):$83,200.00 - $124,800.00This 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 plansIt 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.