New · posted Nov 3
Medtronic · Medical Devices
Senior Clinical Research Specialist
- Fridley, MN +2 more
- On-site
- Full-time
- Senior & Principal
The role
We anticipate the application window for this opening will close on - 9 Nov 2026
Careers 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.
What you need
Required Qualifications
Bachelor’s degree in a technical discipline and 4+ years of relevant clinical research, scientific writing, regulatory writing, or medical device experience; or an advanced degree and 2+ years of relevant experience.
Experience authoring or contributing to clinical, scientific, or regulatory documentation.
Experience supporting cross-functional projects within a regulated healthcare, life sciences, or medical device environment.
Ability to analyze, interpret, and communicate clinical or scientific data to diverse stakeholders.
Preferred Qualificationsnice to have
MD or PhD in a biomedical science discipline.
Experience supporting clinical trials and clinical development programs within the medical device industry.
Experience with clinical, medical, scientific, or regulatory writing and publication development.
Neurovascular, stroke, vascular intervention, or related medical device therapeutic area experience.
Experience supporting regulatory submissions and responses to health authorities.
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.
What you'll do
The Neurovascular Clinical Research team supports the global clinical development of therapies designed to treat stroke and other neurovascular conditions. This team partners across Clinical, Research & Development, Regulatory, Quality, Health Economics & Reimbursement, Marketing, and Medical Affairs to generate clinical evidence that supports product development, regulatory submissions, and commercialization activities.
Primary preference is for candidates based in Fridley/Mounds View, Minnesota OR Irvine, California OR Lafayette, Colorado. This role follows a flexible onsite work model with a minimum of four days per week onsite. Travel requirements are expected to be ~25% based on business needs.
Check us out on LinkedIn: Medtronic Neurovascular
The Senior Clinical Research Specialist supports clinical development programs by leading the development of clinical, scientific, and regulatory documentation while partnering with cross-functional stakeholders to advance evidence generation strategies. This role contributes to study start-up, study execution, publication planning, regulatory submissions, and broader clinical development initiatives supporting neurovascular therapies.
Author and lead the development of clinical, scientific, and regulatory documents, including clinical study protocols, clinical study reports, clinical evaluation reports, annual reports, risk-benefit assessments, and associated submission materials.
Develop clinical evidence strategies and support clinical development activities aligned with program objectives and regulatory requirements.
Partner with cross-functional stakeholders across Clinical, Research & Development, Regulatory Affairs, Quality, Marketing, Sales, Compliance, and Health Economics & Reimbursement to support product development and lifecycle initiatives.
Interpret, analyze, and communicate clinical data through clear and scientifically accurate reports, presentations, and evidence summaries for internal and external audiences.
Conduct scientific literature reviews, clinical evidence assessments, and literature database management activities to support development and regulatory objectives.
Lead publication planning and execution activities in collaboration with physician investigators, key opinion leaders, and internal stakeholders.
Monitor and summarize emerging scientific literature, conference presentations, and competitive developments relevant to the neurovascular therapeutic area.
Manage multiple clinical and business-critical projects simultaneously, coordinating document reviews, stakeholder feedback, revisions, and approval processes.
Pay and benefits
$105,600 – $158,400 a year
Employer providedMedtronic 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
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.
Health, dental and vision insurance
401(k) with employer contribution and match
Paid time off
Employee Stock Purchase Plan
Tuition assistance/reimbursement
Short-term incentive plan (MIP)
Where you'll work
Fridley, MN +2 moreOn-siteOpen in Maps (opens in a new tab)
Also posted for: Lafayette, CO · Irvine, CA
More jobs in Fridley, MN +2 moreWorking conditions
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.
Equal opportunity, accessibility and legal noticesMedtronic's statements, word for word
Recruitment Fraud Alert
We 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 [email protected].
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.
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.
Job intelligence
The context around this role
Live data · November 3, 2026
Salary intelligence
How the pay compares
This role's midpoint is 6% below the US median for Clinical Evaluation & Medical Writing roles at this level.
This roleEmployer provided
Senior & Principal roles in the US13 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $105,600 | — | $158,400 |
| All US (middle half) | $132,000 | $140,000 | $171,000 |
This role: Medtronic's own published range. Comparisons: the base pay employers published on open Clinical Evaluation & Medical Writing roles at the same level on Regulatory Jobs, November 3, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Evaluation & Medical Writing
The general path across 41 open Clinical Evaluation & Medical Writing roles on Regulatory Jobs, with the titles they carry most. Not Medtronic's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 24 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Collaboration and leadership10
- Documentation and SOPs7
- Clinical trial conduct7
- Regulatory submissions4
- GMP and compliance1
- Investigations and CAPA1
Company hiring pulse
Medtronic on Regulatory Jobs
- 27
- Open roles
- 23
- Distinct roles
- 13
- Locations
By discipline
- Quality14 52%
- Regulatory8 30%
- Clinical5 19%
By level
- Senior & Principal15 56%
- Associate & Specialist7 26%
- Manager4 15%
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Senior Clinical Research Specialist at Medtronic
Applications close November 9. $106K–$158K a year, employer provided.