Clinical Research Associate Jobs in Minneapolis, MN
Clinical Research Associate jobs in Minneapolis are concentrated in the medical device and biopharma corridors around the University of Minnesota campus, the Downtown medical district, and the suburban research parks in Plymouth and Eden Prairie, with steady hiring across clinical trials, medical devices, and contract research organizations. Employers hiring right now include University of Minnesota, Medtronic, and Center for Veterans Research and Education. See the openings below and apply to the ones that match your experience.
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Job Title: Research Assistant I
Location: Minneapolis VA Medical Center
Job Code: CRAI, Full Time, Benefit Eligible, Non-Exempt
PI: Diane Mortimer/Casey Gilmore
Project: THIA/ReStart
Summary:
The Center for Veterans Research and Education (CVRE), whose mission is to help support
innovative research and education initiatives that improve the health and well-being of Veterans, is
seeking a Research Assistant.
Position Description:
The Research Assistant is responsible for assisting study investigators and coordinators with the conduct of interventional and observational research studies. Research involves the use of technology including transcranial direct current stimulation (tDCS), electroencephalography (EEG), and magnetic resonance imaging (MRI). This position will require working directly with clinical patients in a research capacity. Clinical populations include traumatic brain injury, substance use, chronic pain, and mood disorders.
Responsibilities:
Major duties and responsibilities may include, but are not limited to, the following:
- Assist with the execution of all aspects of research projects within the PI’s portfolio.
- Assist with recruitment, screening, and medical chart reviews.
- Conduct research study assessments in-person or over the telephone, in accordance with research protocols and standard operating procedures.
- Facilitate follow-up assessment reminders, scheduling, and participant payments.
- Perform data entry for research projects and maintain databases.
- Maintain testing supplies, files, and equipment in an organized manner.
- Maintain awareness of and compliance with research regulatory issues.
- Assist in the preparation of technical reports, summaries, and manuscripts (i.e., literature reviews, table preparation).
- Communicate regularly with study team, under the direction of project leaders, via email and conferencing.
- Maintain professional clearances/human studies training to be fully qualified to work with sensitive data as promulgated by the IRB, HIPAA, VHA, and other regulatory agencies.
- Assist with other research studies or lab duties, as directed by supervisor and as time allows.
Applicant must include a cover letter
Minimum Qualifications:
Education: Bachelor’s (BA/BS) or above from an accredited college or university in
public health, sociology, psychology, or related allied health field
Experience: 0-2 years of experience required for CRA I
2-4 years of experience required for CRA II
Licensure/Registration/Certification: None
Preferred Qualifications:
- Research Assistant experience dealing with data collection and data storage, human subject studies, and institutional review board processes.
- Knowledge of Good Clinical Practices, human subjects’ protections, and federal regulations related to clinical research.
Knowledge, Skills, and Abilities:
- Basic experience with trouble-shooting devices and software settings.
- Experience in coordinating multiple task and project elements with differing timelines and completion deadlines.
- Demonstrated ability to work effectively both independently and as part of a team.
- Excellent oral and written communication skills.
- Exceptional attention to detail and organizational skills.
- Proficiency in Microsoft Office products including Outlook, Word, PowerPoint, and Excel.
Conditions of Employment:
- Subject to a criminal and educational background check.
- Designated and/or random drug testing may be required.
- Regular and predictable attendance is required.
- Typical hours fall within standard business hours, work may be required during hours beyond standard business hours, including weekends.
- Must be a US citizen
Physical Requirements: The employee must be able to navigate the medical center, use a keyboard, and lift 25 lbs. Reasonable accommodation may be considered in determining an applicant’s ability to perform the duties/functions of the position.
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Find JobsClinical Research Associate Job Market in Minneapolis
Who's Hiring
- University of Minnesota12
- Medtronic9
- Center for Veterans Research and Education6C
- AtriCure3
- Headlands Research3
Clinical Research Associate Jobs in Minneapolis: Frequently Asked Questions
How do I get a clinical research associate job in Minneapolis?
Minneapolis clinical research associate hiring is driven by its medical device industry, contract research organizations, and academic medical centers affiliated with the University of Minnesota. Candidates who stand out have hands-on trial monitoring experience, GCP certification, and familiarity with FDA-regulated device or pharmaceutical studies. Targeting the Plymouth and Eden Prairie research corridors alongside Downtown hospital networks gives you the broadest exposure to active openings in this market.
Which companies hire clinical research associates in Minneapolis?
Minneapolis clinical research associate roles are posted by University of Minnesota, Medtronic, and Center for Veterans Research and Education and others right now, based on current listings on Migrate Mate as of October 2026. The local employer mix skews heavily toward medical device manufacturers and the contract research organizations that support them, alongside health system research departments at major Minneapolis teaching hospitals.
Are there remote clinical research associate jobs in Minneapolis?
Yes, though remote availability depends heavily on the role, since site monitoring and on-site trial coordination require in-person presence while data management, regulatory affairs, and study coordination tasks are more remote-compatible. About 71% of clinical research associate openings tied to Minneapolis are remote or hybrid as of October 2026, with the highest remote share in study startup, medical writing, and data review functions. Device-focused monitoring roles in the suburbs tend to require the most on-site time.
How can I get a clinical research associate job in Minneapolis with little or no experience?
The most realistic entry path in Minneapolis is through a clinical research coordinator role at one of the University of Minnesota's affiliated clinical trial sites or a large health system like Hennepin Healthcare. These coordinator positions build the trial management and site monitoring experience that Minneapolis device and CRO employers look for when promoting to associate-level roles. Volunteering or interning in a research department and earning a CCRP credential can accelerate the transition significantly in this market.
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