Clinical Research Jobs in Minnesota
Clinical Research jobs in Minnesota are in strong demand, concentrated in academic medical centers, pharmaceutical research, medical device development, and large integrated health systems across the Twin Cities, Rochester, and Duluth. Mayo Clinic, UnitedHealth Group, and Abbott Laboratories anchor much of the hiring, with additional openings at the University of Minnesota health system and several contract research organizations based in the metro. The most consistently sought specialties include oncology trials, cardiovascular studies, and regulatory affairs coordination. See the openings below and apply to the ones that match your experience.
Find Clinical Research JobsOverview
Showing 5 of 30+ Clinical Research jobs











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
This position will be a full-time S&SS CRS position supporting the CAS Site Management Team.In this exciting role as a Clinical Research Specialist, you will have primary focus responsibility in preparing sites for data collection, relationship building with research coordinators, regulatory report writing, and data cleaning. The CRS works under the direction of a Clinical Study Manager and assists with numerous tasks associated with the execution of a clinical trial.
The Study & Scientific Solutions (S&SS) is a function within Medtronic Core Clinical Solutions (MC2). S&SS is an internal service provider to all of Medtronic and assigns resources to assist Business Units execute on clinical trials and scientific projects when they have an increase in workload.
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 10% of travel to enhance collaboration and ensure successful completion of projects.
Responsibilities may include the following and other duties may be assigned.
Oversees, designs, plans and develops clinical evaluation research studies.
Prepares and authors protocols and patient record forms.
Conducts registered and non-registered clinical studies of products that have been determined to satisfy a medical need and/or offer a commercial potential.
Oversees and interpret results of clinical investigations in preparation for new drug device or consumer application.
Oversees 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.
May be responsible for clinical supply operations, site and vendor selection.
People working within region/country may also have the responsibilities that include:
Represents Medtronic from a clinical research respective within the country / region and also collects feedback from local customers and authorities.
Builds and maintains optimal relationships and effective collaborations with various internal and external parties.
Drives local evidence dissemination & awareness.
Minimum Requirements:
Bachelor's degree plus 2+ years of clinical site management experience
Nice to Have:
Bachelor's degree in degree in engineering, life sciences, or related medical/scientific field
Previous Medtronic experience
Clinical experience
Site Management experience (site or sponsor)
Knowledge of/experience with CTMS/EDC/TMF
Experience with Good Clinical Practice (GCP)
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.
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.
See All 30 Clinical Research Jobs in Minnesota
Find roles in Minnesota that match your experience and apply in just a few clicks.
Find Clinical Research JobsClinical Research Jobs by City in Minnesota
Where Minnesota roles are concentrated, by current openings.
Clinical Research Job Market in Minnesota
A snapshot from current Minnesota openings, updated as new roles post.
Who's Hiring



Top Industries Hiring
- Education
- Medical Devices
- Distribution & Wholesale
What Minnesota Employers Look For
The qualifications that appear most often in clinical research jobs across Minnesota.
- Bachelor's degree in life sciences, nursing, or a related clinical field required
- Experience with Good Clinical Practice (GCP) guidelines and ICH standards
- Proficiency in electronic data capture systems such as Medidata Rave or REDCap
- Familiarity with IRB submission processes and informed consent procedures
- Strong documentation skills and attention to detail for regulatory compliance
- Ability to coordinate across multidisciplinary teams including physicians and sponsors
Clinical Research Jobs in Minnesota: Frequently Asked Questions
How do you become a clinical research in Minnesota?
Most clinical research positions in Minnesota require a bachelor's degree in a life science, nursing, or health-related field, followed by entry-level experience in a clinical or laboratory setting. While Minnesota does not issue a state-specific license for clinical research coordinators, many employers expect candidates to hold or pursue the Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) credential through the Society of Clinical Research Associates or the Association of Clinical Research Professionals.
Which companies hire clinical researchs in Minnesota?
Employers hiring clinical researchs in Minnesota right now include University of Minnesota, Mayo Clinic, and Medtronic, based on current listings on Migrate Mate as of August 2026. Minnesota's deep concentration of medical device manufacturers, large health systems, and contract research organizations creates unusually consistent demand throughout the year.
Which Minnesota cities have the most clinical research jobs?
The cities with the most clinical research openings in Minnesota are Minneapolis, Rochester, and Minnesota. The Minneapolis-Saint Paul metro drives the bulk of listings because of its density of academic medical centers, medical device headquarters, and contract research organizations, while Rochester's concentration around Mayo Clinic supports a strong secondary market for trial coordination and data management roles.
Are there remote clinical research jobs in Minnesota?
Yes, but they're limited. About 53% of clinical research openings tied to Minnesota are remote or hybrid as of August 2026, reflecting the field's frequent need for on-site patient interaction and specimen handling. Roles most likely to be fully remote are those focused on regulatory writing, clinical data management, and sponsor monitoring oversight rather than direct patient-facing coordination.
How can I get hired as a clinical research in Minnesota with little or no experience?
The most realistic entry path is a research coordinator assistant or clinical trials assistant role at one of Minnesota's major academic health systems, including Mayo Clinic or M Health Fairview, both of which post new-grad-accessible positions that provide supervised GCP training. Candidates coming from nursing, pharmacy technician, or medical assistant backgrounds have a clear lateral path into coordinator roles. Completing an online GCP certification through the National Institutes of Health or enrolling in the University of Minnesota's clinical research certificate program strengthens an application considerably before a first hire.
Where can I find and apply to clinical research jobs in Minnesota?
You can find and apply to clinical research jobs in Minnesota on Migrate Mate, which lists current openings from employers actively hiring in the state. Search the listings to find roles that match your experience level and specialty area, then apply directly to the ones that fit.
See All 30 Clinical Research Jobs in Minnesota
Find roles in Minnesota that match your experience and apply in just a few clicks.
Find Clinical Research Jobs