TN Visa Research Specialist Jobs
Research Specialist roles qualify for TN visa sponsorship under the USMCA's Scientific Technician/Technologist and Social Science categories, depending on your credentials and research domain. Canadian citizens can apply at the port of entry with no cap concerns. Mexican nationals go through consular processing with an annual allocation.
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We anticipate the application window for this opening will close on - 4 May 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
As one of three comprehensive portfolios at Medtronic, Neuroscience is dedicated to improving the lives of people living with neurological disorders, spine conditions, and chronic pain. Guided by our Mission—to alleviate pain, restore health, and extend life—we develop technologies and therapies that help people regain function, reduce pain, and return to the activities that matter most.
Our Cranial & Spinal Technologies (CST) operating unit advances surgical care for spine and cranial conditions through an integrated ecosystem of implants, navigation, robotics, imaging, and planning tools. Platforms like AiBLE enhance precision, efficiency, and outcomes for complex procedures worldwide.
In this role as Associate Clinical Research Specialist (Associate CRS), you will support the execution of post-market clinical trials within Medtronic’s CST portfolio. You will primarily be responsible for investigative site management, including training site research staff and ensuring study data is accurate, complete, and of high quality. You will partner closely with internal clinical teams and external investigative sites to ensure studies are conducted in compliance with applicable regulations, Good Clinical Practice (GCP), and Medtronic standard operating procedures (SOPs).
Key Responsibilities include (but are not limited to):
- Supports the execution of registered and non-registered clinical studies for products addressing medical needs and/or commercial opportunities.
- Assists in the review and interpretation of clinical investigation results to support regulatory and product development activities.
- Helps manage operational aspects of clinical trials in collaboration with project teams, ensuring compliance with SOPs, GCP, and country-specific regulations; may support clinical trial budget activities.
- May assist with clinical supply operations, as well as site and vendor selection.
-
Contributes to regional or country-specific activities, including:
-
Representing Medtronic from a clinical research perspective and gathering feedback from local customers and regulatory authorities.
- Building and maintaining effective relationships with internal and external stakeholders.
- Supporting local evidence dissemination and awareness efforts.
Location: Remote within US – Upper Midwest region.
- This position is primarily remote, with occasional travel to investigative sites and/or Medtronic facilities as business needs require.
Remote: We are seeking a committed professional to join our team, required to reside within the territory and drive to multiple accounts throughout the region. A valid driver's license is essential for this role, which also involves 25% of travel outside the territory, presenting opportunities for broader engagement.
Required Qualifications
- Bachelor’s degree in Life Science, Health Science, Engineering or related field is required with a minimum of 0 years of experience.
- Broad theoretical knowledge of clinical research principles obtained through academic training.
- Ability to work autonomously in a remote environment while maintaining effective collaboration.
Preferred Qualifications
- Academic or internship exposure to clinical research, GCP, or regulated environments.
- Strong attention to detail and analytical skills for data review and quality oversight.
- Effective written and verbal communication skills and comfort engaging with investigative site staff.
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): $65,600.00 - $98,400.00
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:
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.
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 - 4 May 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
As one of three comprehensive portfolios at Medtronic, Neuroscience is dedicated to improving the lives of people living with neurological disorders, spine conditions, and chronic pain. Guided by our Mission—to alleviate pain, restore health, and extend life—we develop technologies and therapies that help people regain function, reduce pain, and return to the activities that matter most.
Our Cranial & Spinal Technologies (CST) operating unit advances surgical care for spine and cranial conditions through an integrated ecosystem of implants, navigation, robotics, imaging, and planning tools. Platforms like AiBLE enhance precision, efficiency, and outcomes for complex procedures worldwide.
In this role as Associate Clinical Research Specialist (Associate CRS), you will support the execution of post-market clinical trials within Medtronic’s CST portfolio. You will primarily be responsible for investigative site management, including training site research staff and ensuring study data is accurate, complete, and of high quality. You will partner closely with internal clinical teams and external investigative sites to ensure studies are conducted in compliance with applicable regulations, Good Clinical Practice (GCP), and Medtronic standard operating procedures (SOPs).
Key Responsibilities include (but are not limited to):
- Supports the execution of registered and non-registered clinical studies for products addressing medical needs and/or commercial opportunities.
- Assists in the review and interpretation of clinical investigation results to support regulatory and product development activities.
- Helps manage operational aspects of clinical trials in collaboration with project teams, ensuring compliance with SOPs, GCP, and country-specific regulations; may support clinical trial budget activities.
- May assist with clinical supply operations, as well as site and vendor selection.
-
Contributes to regional or country-specific activities, including:
-
Representing Medtronic from a clinical research perspective and gathering feedback from local customers and regulatory authorities.
- Building and maintaining effective relationships with internal and external stakeholders.
- Supporting local evidence dissemination and awareness efforts.
Location: Remote within US – Upper Midwest region.
- This position is primarily remote, with occasional travel to investigative sites and/or Medtronic facilities as business needs require.
Remote: We are seeking a committed professional to join our team, required to reside within the territory and drive to multiple accounts throughout the region. A valid driver's license is essential for this role, which also involves 25% of travel outside the territory, presenting opportunities for broader engagement.
Required Qualifications
- Bachelor’s degree in Life Science, Health Science, Engineering or related field is required with a minimum of 0 years of experience.
- Broad theoretical knowledge of clinical research principles obtained through academic training.
- Ability to work autonomously in a remote environment while maintaining effective collaboration.
Preferred Qualifications
- Academic or internship exposure to clinical research, GCP, or regulated environments.
- Strong attention to detail and analytical skills for data review and quality oversight.
- Effective written and verbal communication skills and comfort engaging with investigative site staff.
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): $65,600.00 - $98,400.00
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:
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.
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.
See all 656+ Research Specialist jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Research Specialist roles.
Get Access To All JobsTips for Finding TN Visa Sponsorship as a Research Specialist
Align your credentials to the right TN category
Research Specialist spans multiple TN categories. A social science researcher qualifies differently than a life sciences technician. Confirm your degree field matches the specific TN category your role falls under before starting any application.
Target employers with established research infrastructure
Universities, federal contract research organizations, and pharmaceutical firms hire Research Specialists regularly under TN. These employers already understand sponsorship paperwork and won't need to be educated on the visa process during negotiations.
Request an offer letter that specifies your research activities
Generic offer letters cause TN denials at the border. The letter must describe your actual research duties, the scientific or social science field involved, and confirm the role requires your specific degree. Vague language like 'research support' is a common rejection trigger.
Use Migrate Mate to find Research Specialist roles with active TN sponsorship
Filtering job listings by TN visa eligibility saves weeks of outreach to employers unfamiliar with the category. Migrate Mate surfaces Research Specialist openings from employers already set up to sponsor TN applicants in your field.
Prepare documentation proving research qualifies as specialty practice
CBP officers may challenge whether a Research Specialist role constitutes professional practice under the TN categories. Bring published work, institutional affiliation letters, or a detailed job description tying your duties to a recognized scientific discipline.
Clarify your TN status intent before accepting multi-site roles
Research Specialists who work across multiple institutional sites or under subcontracts need the TN petition to reflect all work locations. A single-site approval that doesn't match your actual work arrangement can create compliance problems at renewal.
Research Specialist jobs are hiring across the US. Find yours.
Find Research Specialist JobsResearch Specialist TN Visa: Frequently Asked Questions
Does a Research Specialist role qualify for a TN visa?
It depends on the research domain and your credentials. Research Specialists in life sciences, social sciences, agriculture, and related fields can qualify under TN categories like Scientific Technician/Technologist or Social Science if the role requires a relevant bachelor's degree or higher and your duties align with professional practice in that discipline. Roles that are primarily administrative or involve general data entry won't qualify.
How does TN compare to H-1B for Research Specialist positions?
TN has no annual lottery, no cap for Canadians, and can be approved at the port of entry the same day. H-1B requires a March lottery registration with roughly a one-in-four selection chance, followed by months of USCIS processing. For Canadian Research Specialists with a qualifying degree and a compliant job offer, TN is faster and more predictable. Mexican nationals face an annual TN allocation, but consular processing still avoids the H-1B lottery entirely.
Can I search for Research Specialist jobs that already support TN sponsorship?
Yes. Migrate Mate lets you filter Research Specialist listings by TN visa eligibility, so you're only seeing employers who are set up to sponsor the category. This avoids the common situation where you reach an offer stage only to learn the employer has never filed a TN petition and isn't willing to start.
What documents does a Mexican national need for TN Research Specialist sponsorship?
Mexican nationals apply for TN status at a U.S. consulate, not at the border. You'll need a valid Mexican passport, the DS-160 nonimmigrant visa application, the MRV fee receipt, a compliant employer offer letter specifying your research duties and required degree, and your educational credentials. The consulate may also request evidence of the employer's legitimacy, such as business registration documents or financial statements.
What makes a Research Specialist TN application fail at the border or consulate?
The most common failure points are an offer letter that describes duties too broadly, a degree field that doesn't map clearly to the TN category listed, and roles where the research work could be performed without a specialized degree. CBP officers and consular officers both apply the specialty occupation standard. Bringing published research, a detailed position description, and transcripts that directly connect your degree to the job duties reduces rejection risk significantly.
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