Clinical Research Visa Sponsorship Jobs in Minnesota
Minnesota's clinical research sector is anchored by Mayo Clinic in Rochester, the University of Minnesota Medical School, and a growing cluster of medical device and biopharma companies in the Twin Cities. Organizations like Medtronic, Pfizer, and Boston Scientific actively recruit for clinical research roles, and many sponsor international candidates through H-1B visa and other work visa programs.
Find Clinical Research JobsOverview
Showing 5 of 31+ Clinical Research Jobs in Minnesota with Visa Sponsorship
See all 31+ Clinical Research Jobs in Minnesota with Visa Sponsorship
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Clinical Research Jobs in Minnesota with Visa Sponsorship.
Get Access To All JobsWe anticipate the application window for this opening will close on - 17 Oct 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.
A Day in the Life
At Medtronic Neuroscience, we bring innovation, expertise, and purpose together to improve care for people living with neurological, spinal, and chronic pain conditions. Our technologies help restore function, improve quality of life, and support better outcomes for patients around the world.
The Neurovascular Operating Unit develops device-based therapies and technologies that support the diagnosis, treatment, and management of neurovascular conditions. The team partners across clinical, regulatory, medical, and product development functions to generate clinical evidence that supports product development, regulatory submissions, and patient access to therapy.
Preference for this position is Fridley, MN, Irvine, CA or Lafayette, CO. If the selected candidate is subject to local Return to Office requirements, those requirements will be followed.
The Clinical Research Specialist supports the execution of clinical studies within the Neurovascular Operating Unit. Working closely with Clinical Study Managers and cross-functional partners, this role is responsible for clinical site management, study documentation, data quality activities, and operational support to ensure studies are conducted in compliance with applicable regulations, study protocols, and internal requirements.
Primary Responsibilities
- Manage clinical study sites from activation through closeout, including site initiation, training, issue resolution, and ongoing support.
- Review, approve, and maintain regulatory and study-startup documentation to support site activation and continued compliance.
- Coordinate investigator and site staff activities to ensure protocol adherence, data quality, and achievement of study objectives.
- Maintain clinical study files, essential documentation, training materials, and study records.
- Review clinical data, resolve data discrepancies, track open queries, and partner with monitors to address study action items.
- Support development and execution of clinical management plans, protocols, case report forms, and study-related documentation.
- Monitor study progress and prepare reports on clinical investigation activities, milestones, and results.
- Collaborate with internal and external stakeholders, including study sites, vendors, and cross-functional teams, to support successful study execution.
Required Qualifications
- High School Diploma (or equivalent) and 6+ years OR Associate's Degree and 4+ years OR Bachelor's Degree and 2+ years OR Advanced Degree in clinical research, clinical operations, or related clinical study support experience.
- Experience supporting clinical studies and clinical site management activities.
- Experience working in compliance with Good Clinical Practice (GCP) requirements.
- Experience reviewing clinical data, resolving discrepancies, and maintaining study documentation.
Preferred Qualifications
- Degree in Engineering, Life Sciences, or a medical/scientific discipline.
- Certified Clinical Research Associate (CCRA) or Society of Clinical Research Associates (SOCRA) certification.
- Clinical research experience within the medical device industry.
- Experience managing multiple clinical research sites and supporting clinical operations activities.
- Knowledge of clinical research regulations and standards, including International Council for Harmonisation (ICH), Food and Drug Administration (FDA), Medical Device Regulation (MDR), and International Organization for Standardization (ISO) requirements.
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.
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 AskHR@medtronic.com.
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): $83,200.00 - $124,800.00
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
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.
We anticipate the application window for this opening will close on - 17 Oct 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.
A Day in the Life
At Medtronic Neuroscience, we bring innovation, expertise, and purpose together to improve care for people living with neurological, spinal, and chronic pain conditions. Our technologies help restore function, improve quality of life, and support better outcomes for patients around the world.
The Neurovascular Operating Unit develops device-based therapies and technologies that support the diagnosis, treatment, and management of neurovascular conditions. The team partners across clinical, regulatory, medical, and product development functions to generate clinical evidence that supports product development, regulatory submissions, and patient access to therapy.
Preference for this position is Fridley, MN, Irvine, CA or Lafayette, CO. If the selected candidate is subject to local Return to Office requirements, those requirements will be followed.
The Clinical Research Specialist supports the execution of clinical studies within the Neurovascular Operating Unit. Working closely with Clinical Study Managers and cross-functional partners, this role is responsible for clinical site management, study documentation, data quality activities, and operational support to ensure studies are conducted in compliance with applicable regulations, study protocols, and internal requirements.
Primary Responsibilities
- Manage clinical study sites from activation through closeout, including site initiation, training, issue resolution, and ongoing support.
- Review, approve, and maintain regulatory and study-startup documentation to support site activation and continued compliance.
- Coordinate investigator and site staff activities to ensure protocol adherence, data quality, and achievement of study objectives.
- Maintain clinical study files, essential documentation, training materials, and study records.
- Review clinical data, resolve data discrepancies, track open queries, and partner with monitors to address study action items.
- Support development and execution of clinical management plans, protocols, case report forms, and study-related documentation.
- Monitor study progress and prepare reports on clinical investigation activities, milestones, and results.
- Collaborate with internal and external stakeholders, including study sites, vendors, and cross-functional teams, to support successful study execution.
Required Qualifications
- High School Diploma (or equivalent) and 6+ years OR Associate's Degree and 4+ years OR Bachelor's Degree and 2+ years OR Advanced Degree in clinical research, clinical operations, or related clinical study support experience.
- Experience supporting clinical studies and clinical site management activities.
- Experience working in compliance with Good Clinical Practice (GCP) requirements.
- Experience reviewing clinical data, resolving discrepancies, and maintaining study documentation.
Preferred Qualifications
- Degree in Engineering, Life Sciences, or a medical/scientific discipline.
- Certified Clinical Research Associate (CCRA) or Society of Clinical Research Associates (SOCRA) certification.
- Clinical research experience within the medical device industry.
- Experience managing multiple clinical research sites and supporting clinical operations activities.
- Knowledge of clinical research regulations and standards, including International Council for Harmonisation (ICH), Food and Drug Administration (FDA), Medical Device Regulation (MDR), and International Organization for Standardization (ISO) requirements.
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.
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 AskHR@medtronic.com.
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): $83,200.00 - $124,800.00
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
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.
Clinical Research Job Roles in Minnesota
See all 31+ Clinical Research Jobs in Minnesota
Sign up for free to filter by visa type, set job alerts, and find employers with verified sponsorship history.
Search Clinical Research Jobs in MinnesotaClinical Research Jobs in Minnesota: Frequently Asked Questions
Which companies sponsor visas for clinical research roles in Minnesota?
Mayo Clinic, Medtronic, UnitedHealth Group, Boston Scientific, and the University of Minnesota are among the most consistent sponsors for clinical research positions in Minnesota. Academic medical centers and large medical device companies tend to have established immigration programs and legal infrastructure to support H-1B and other work visa petitions, making them more predictable sponsors than smaller CROs or startups.
Which visa types are most common for clinical research roles in Minnesota?
The H-1B is the most common visa for clinical research coordinators, clinical trial managers, and biostatisticians in Minnesota, as these roles typically require a bachelor's degree or higher in a relevant field such as life sciences, nursing, or statistics. Researchers at academic institutions may also qualify for J-1 visa exchange visitor status or, for those with exceptional research records, the O-1A visa for extraordinary ability.
Which cities in Minnesota have the most clinical research sponsorship jobs?
The Twin Cities metro area, particularly Minneapolis and its surrounding suburbs like Plymouth and Maple Grove, concentrates the largest share of clinical research sponsorship jobs due to the presence of medical device headquarters and large health systems. Rochester is also a significant hub given Mayo Clinic's scale of clinical operations, regularly recruiting for clinical research coordinator and regulatory affairs roles with visa sponsorship.
How to find clinical research visa sponsorship jobs in Minnesota?
Migrate Mate filters job listings specifically by visa sponsorship availability, so you can search clinical research roles in Minnesota without sorting through positions that don't support international candidates. The platform covers roles across Mayo Clinic, Twin Cities medical device companies, and academic health systems, making it practical for clinical research professionals on H-1B or other work visas to identify employers actively hiring and sponsoring.
Are there any state-specific considerations for clinical research professionals seeking sponsorship in Minnesota?
Minnesota's concentration of medical device companies under FDA oversight means many clinical research roles require familiarity with GCP guidelines and FDA regulatory submissions, which can strengthen an H-1B petition by demonstrating the specialized nature of the position. The University of Minnesota's clinical and translational research programs also create a steady pipeline of international researchers who pursue H-1B sponsorship after completing OPT or J-1 exchange appointments.
What is the prevailing wage for sponsored clinical research jobs in Minnesota?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.