Research Associate Visa Sponsorship Jobs in Michigan
Michigan's research associate roles are concentrated in life sciences, automotive R&D, and academic medicine, with major employers including the University of Michigan, Michigan State University, Pfizer's Ann Arbor operations, and Henry Ford Health. Ann Arbor, Detroit, and East Lansing anchor most sponsorship activity in the state.
Find Research Associate JobsOverview
Showing 5 of 490+ Research Associate Jobs in Michigan with Visa Sponsorship
See all 490+ Research Associate Jobs in Michigan with Visa Sponsorship
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Research Associate Jobs in Michigan with Visa Sponsorship.
Get Access To All JobsJob Summary
This position will serve as a Clinical Research Coordinator Associate (may be underfilled at Clinical Research Coordinator Technician or Assistant). The position is within the Division of Metabolism, Endocrinology, and Diabetes (MEND) and will provide study coordination support to University of Michigan faculty and research teams specializing in diabetes research. The Clinical Research Coordinator (CRC) may coordinate multiple clinical research studies ranging from moderate to complex.
We seek candidates who can perform clinical research tasks independently, efficiently, and accurately to produce high-quality work, as well as those who are interested in mastering these skills. Given the nature of the research activities, the ideal candidate will be technologically proficient, particularly with digital, mobile, and computer-based systems, and will have flexibility in their working hours. Candidates should be able (or willing to develop the ability) to perform most tasks independently, conduct quality checks of their own work, identify and use appropriate resources and support, and recognize when to escalate issues requiring additional intervention.
Responsibilities
Main responsibilities and Characteristic Duties:
- Develop and maintain an understanding of study-related concepts, including research design and diabetes
- Recruit research participants
- Conduct participant outreach and communication
- Schedule participant visits and complete follow-up activities
- Collect data, including through verbally administered surveys
- Enter and upload data and perform quality assurance checks
- Complete study-related documentations
- Communicate effectively with the study team, including attending weekly team meetings
- Perform participant safety-related responsibilities, including distinguishing among adverse events (AEs), serious adverse events (SAEs), and other reportable information and occurrences (ORIOs), and reporting them appropriately
We maintain high expectations for ethical conduct, professionalism, effective communication, and teamwork.
Supervision Received:
This position receives direct supervision from the program manager and faculty principal investigator.
Supervision Exercised:
None
Additional expectation based on career level:
Clinical Research Coordinator - Associate: This position should demonstrate understanding of protocol elements/requirements and demonstrates the ability to execute study procedures.
- Demonstrates the ability to anticipate and mitigate the potential for protocol non-compliance.
- Describes protocol structure and explains how to interpret study requirements to ensure study compliance.
- Demonstrates accurate implementation of protocol procedures.
- Explains and performs non-GCP-related study management activities.
- Performs study procedures with minimal supervision.
- Triages simple subject issues appropriately.
May fill with an underfill position based on qualified candidate:
Clinical Research Coordinator - Technician: This position may independently provide study coordination for simple and moderately complex clinical research studies. Mastery of all job duties from the Clinical Research Assistant position is required.
- Performs moderately complex study procedures with accuracy.
- Triages simple subject concerns appropriately.
- Assesses studies for execution and troubleshoots potential implementation issues.
- Completes simple to moderately complex data collection during study visits.
- Assists with quality control efforts.
- Performs study procedures with accuracy.
- Triages simple subject concerns appropriately.
- Assesses studies for execution and troubleshoots potential implementation issues.
- Completes simple data collection during study visits.
- Assists with quality control efforts.
Clinical Research Coordinator - Assistant: This position will assist with study coordination for simple clinical research studies.
Required Qualifications
Clinical Research Coordinator - Associate
- Bachelor's Degree in Health Science or equivalent in combined education and clinical research experience.
- Certification is required through Association of Clinical Research Professionals (ACRP) as a Certified Clinical Research Coordinator (CCRC) or Society of Clinical Research Association (SOCRA) as a Certified Clinical Research Professionals (CCRP) or equivalent. Candidates must be eligible to register or take the exam at date of hire and the certification must be completed or passed etc. within six months of date of hire. (Please review eligibility criteria from SOCRA or ACRP)
- Minimum 2 years of directly related experience in clinical research and clinical trials is necessary. Please review SOCRA's Definition of a Clinical Research Professional qualifying experience prior to applying.
Underfill Qualifications:
Clinical Research Coordinator - Technician
- Associate Degree in Health Science or an equivalent combination of related education and experience is necessary.
- ONE of the following:
- Minimum 1 year of directly related experience in clinical research and clinical trials is necessary. Please review SoCRA's Definition of a Clinical Research Professional qualifying experience prior to applying.
- An advanced degree in a health-related area such as: Health Sciences, Behavioral Sciences, Public Health, Health Care Administration, Clinical Research Administration, Social Work, Psychology, Epidemiology, Foreign MD.
- Minimum 3 years of human subject experience (clinical, lab or health regulations) such as related patient care, related community health and wellness, related clinical information, and research.
- High school diploma or GED is necessary.
Clinical Research Coordinator - Assistant
- High school diploma or GED is necessary.
Desired Qualifications
Clinical Research Coordinator - Associate
- 4+ years of direct related experience.
- Bachelor's Degree; Health Science field preferred or related certification.
- Understanding of medical terminology.
- Experience in a large, complex, healthcare setting.
- Ability to effectively communicate with staff and faculty of all levels.
- Knowledge of University policies and procedures.
Clinical Research Coordinator - Technician
- Bachelor's Degree; Health Science field preferred or related certification.
- Understanding of medical terminology.
- Experience in a large, complex, healthcare setting.
- Ability to effectively communicate with staff and faculty of all levels.
- Knowledge of University policies and procedures.
Clinical Research Coordinator - Assistant
- Bachelor's Degree; Health Science field preferred or related certification.
- An understanding of medical terminology, experience in a large complex health care setting, ability to effectively communicate with staff and faculty of all levels, and knowledge of university policies and procedures is desirable.
Modes of Work
Positions that are eligible for hybrid or mobile/remote work mode are at the discretion of the hiring department. Work agreements are reviewed annually at a minimum and are subject to change at any time, and for any reason, throughout the course of employment. Learn more about the work modes.
Work Schedule
Positions may be eligible for hybrid work. Work agreements will be reviewed annually at a minimum and are subject to change at any time, and for any reason, throughout the course of employment. Learn more about the work modes. Work hours will be flexible. A combination of core business hours (Monday through Friday 9am-5pm) and weekend and evening hours will be required to support study requirements. Primary work location is at Domino's Farms in Ann Arbor.
Background Screening
Michigan Medicine conducts background screening and pre-employment drug testing on job candidates upon acceptance of a contingent job offer and may use a third party administrator to conduct background screenings. Background screenings are performed in compliance with the Fair Credit Report Act. Pre-employment drug testing applies to all selected candidates, including new or additional faculty and staff appointments, as well as transfers from other U-M campuses.
U-M EEO Statement
The University of Michigan is an Equal Opportunity Employer. We are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants, including protected veterans and individuals with disabilities.
Job Opening ID
282865
Working Title
Clinical Research Coordinator Associate (underfill Technician or Assistant)
Job Title
Clinical Research Coord Assoc
Work Location
Ann Arbor Campus
Ann Arbor, MI
Modes of Work
Onsite
Full/Part Time
Full-Time
Regular/Temporary
Regular
FLSA Status
Nonexempt
Organizational Group
Medical School
Department
MM Metabolism, Endo & Diabetes
Posting Begin/End Date
9/11/2026 - 9/25/2026
Career Interest
Research
Job Summary
This position will serve as a Clinical Research Coordinator Associate (may be underfilled at Clinical Research Coordinator Technician or Assistant). The position is within the Division of Metabolism, Endocrinology, and Diabetes (MEND) and will provide study coordination support to University of Michigan faculty and research teams specializing in diabetes research. The Clinical Research Coordinator (CRC) may coordinate multiple clinical research studies ranging from moderate to complex.
We seek candidates who can perform clinical research tasks independently, efficiently, and accurately to produce high-quality work, as well as those who are interested in mastering these skills. Given the nature of the research activities, the ideal candidate will be technologically proficient, particularly with digital, mobile, and computer-based systems, and will have flexibility in their working hours. Candidates should be able (or willing to develop the ability) to perform most tasks independently, conduct quality checks of their own work, identify and use appropriate resources and support, and recognize when to escalate issues requiring additional intervention.
Responsibilities
Main responsibilities and Characteristic Duties:
- Develop and maintain an understanding of study-related concepts, including research design and diabetes
- Recruit research participants
- Conduct participant outreach and communication
- Schedule participant visits and complete follow-up activities
- Collect data, including through verbally administered surveys
- Enter and upload data and perform quality assurance checks
- Complete study-related documentations
- Communicate effectively with the study team, including attending weekly team meetings
- Perform participant safety-related responsibilities, including distinguishing among adverse events (AEs), serious adverse events (SAEs), and other reportable information and occurrences (ORIOs), and reporting them appropriately
We maintain high expectations for ethical conduct, professionalism, effective communication, and teamwork.
Supervision Received:
This position receives direct supervision from the program manager and faculty principal investigator.
Supervision Exercised:
None
Additional expectation based on career level:
Clinical Research Coordinator - Associate: This position should demonstrate understanding of protocol elements/requirements and demonstrates the ability to execute study procedures.
- Demonstrates the ability to anticipate and mitigate the potential for protocol non-compliance.
- Describes protocol structure and explains how to interpret study requirements to ensure study compliance.
- Demonstrates accurate implementation of protocol procedures.
- Explains and performs non-GCP-related study management activities.
- Performs study procedures with minimal supervision.
- Triages simple subject issues appropriately.
May fill with an underfill position based on qualified candidate:
Clinical Research Coordinator - Technician: This position may independently provide study coordination for simple and moderately complex clinical research studies. Mastery of all job duties from the Clinical Research Assistant position is required.
- Performs moderately complex study procedures with accuracy.
- Triages simple subject concerns appropriately.
- Assesses studies for execution and troubleshoots potential implementation issues.
- Completes simple to moderately complex data collection during study visits.
- Assists with quality control efforts.
- Performs study procedures with accuracy.
- Triages simple subject concerns appropriately.
- Assesses studies for execution and troubleshoots potential implementation issues.
- Completes simple data collection during study visits.
- Assists with quality control efforts.
Clinical Research Coordinator - Assistant: This position will assist with study coordination for simple clinical research studies.
Required Qualifications
Clinical Research Coordinator - Associate
- Bachelor's Degree in Health Science or equivalent in combined education and clinical research experience.
- Certification is required through Association of Clinical Research Professionals (ACRP) as a Certified Clinical Research Coordinator (CCRC) or Society of Clinical Research Association (SOCRA) as a Certified Clinical Research Professionals (CCRP) or equivalent. Candidates must be eligible to register or take the exam at date of hire and the certification must be completed or passed etc. within six months of date of hire. (Please review eligibility criteria from SOCRA or ACRP)
- Minimum 2 years of directly related experience in clinical research and clinical trials is necessary. Please review SOCRA's Definition of a Clinical Research Professional qualifying experience prior to applying.
Underfill Qualifications:
Clinical Research Coordinator - Technician
- Associate Degree in Health Science or an equivalent combination of related education and experience is necessary.
- ONE of the following:
- Minimum 1 year of directly related experience in clinical research and clinical trials is necessary. Please review SoCRA's Definition of a Clinical Research Professional qualifying experience prior to applying.
- An advanced degree in a health-related area such as: Health Sciences, Behavioral Sciences, Public Health, Health Care Administration, Clinical Research Administration, Social Work, Psychology, Epidemiology, Foreign MD.
- Minimum 3 years of human subject experience (clinical, lab or health regulations) such as related patient care, related community health and wellness, related clinical information, and research.
- High school diploma or GED is necessary.
Clinical Research Coordinator - Assistant
- High school diploma or GED is necessary.
Desired Qualifications
Clinical Research Coordinator - Associate
- 4+ years of direct related experience.
- Bachelor's Degree; Health Science field preferred or related certification.
- Understanding of medical terminology.
- Experience in a large, complex, healthcare setting.
- Ability to effectively communicate with staff and faculty of all levels.
- Knowledge of University policies and procedures.
Clinical Research Coordinator - Technician
- Bachelor's Degree; Health Science field preferred or related certification.
- Understanding of medical terminology.
- Experience in a large, complex, healthcare setting.
- Ability to effectively communicate with staff and faculty of all levels.
- Knowledge of University policies and procedures.
Clinical Research Coordinator - Assistant
- Bachelor's Degree; Health Science field preferred or related certification.
- An understanding of medical terminology, experience in a large complex health care setting, ability to effectively communicate with staff and faculty of all levels, and knowledge of university policies and procedures is desirable.
Modes of Work
Positions that are eligible for hybrid or mobile/remote work mode are at the discretion of the hiring department. Work agreements are reviewed annually at a minimum and are subject to change at any time, and for any reason, throughout the course of employment. Learn more about the work modes.
Work Schedule
Positions may be eligible for hybrid work. Work agreements will be reviewed annually at a minimum and are subject to change at any time, and for any reason, throughout the course of employment. Learn more about the work modes. Work hours will be flexible. A combination of core business hours (Monday through Friday 9am-5pm) and weekend and evening hours will be required to support study requirements. Primary work location is at Domino's Farms in Ann Arbor.
Background Screening
Michigan Medicine conducts background screening and pre-employment drug testing on job candidates upon acceptance of a contingent job offer and may use a third party administrator to conduct background screenings. Background screenings are performed in compliance with the Fair Credit Report Act. Pre-employment drug testing applies to all selected candidates, including new or additional faculty and staff appointments, as well as transfers from other U-M campuses.
U-M EEO Statement
The University of Michigan is an Equal Opportunity Employer. We are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants, including protected veterans and individuals with disabilities.
Job Opening ID
282865
Working Title
Clinical Research Coordinator Associate (underfill Technician or Assistant)
Job Title
Clinical Research Coord Assoc
Work Location
Ann Arbor Campus
Ann Arbor, MI
Modes of Work
Onsite
Full/Part Time
Full-Time
Regular/Temporary
Regular
FLSA Status
Nonexempt
Organizational Group
Medical School
Department
MM Metabolism, Endo & Diabetes
Posting Begin/End Date
9/11/2026 - 9/25/2026
Career Interest
Research
Research Associate Job Roles in Michigan
See all 490+ Research Associate Jobs in Michigan
Sign up for free to filter by visa type, set job alerts, and find employers with verified sponsorship history.
Search Research Associate Jobs in MichiganResearch Associate Jobs in Michigan: Frequently Asked Questions
Which companies sponsor visas for research associates in Michigan?
The University of Michigan and Michigan State University are among the most active sponsors, given their large research programs in biomedical sciences, engineering, and social sciences. Henry Ford Health, Spectrum Health, and pharmaceutical operations in the Ann Arbor and Detroit metro areas also have established sponsorship histories. Large automotive manufacturers with dedicated R&D divisions, such as General Motors and Ford, sponsor research associates in materials science and engineering disciplines.
Which visa types are most common for research associate roles in Michigan?
The H-1B visa is the most common visa for research associates in Michigan, as most positions require at least a bachelor's degree in a specific field, satisfying the specialty occupation standard. J-1 visa research scholar status is also widely used, particularly at university and hospital settings. Candidates with extraordinary ability in their research field may qualify for the O-1 visa. Nationals of Canada and Mexico may pursue TN visa status if the role fits a qualifying TN occupational category.
Which cities in Michigan have the most research associate sponsorship jobs?
Ann Arbor has the highest concentration of research associate sponsorship activity, driven by the University of Michigan's extensive research enterprise and surrounding life sciences companies. East Lansing follows due to Michigan State University's research programs. Detroit and its suburbs attract sponsorship through hospital systems, automotive R&D centers, and contract research organizations. Grand Rapids also has a growing presence through Spectrum Health and regional pharmaceutical employers.
How to find research associate visa sponsorship jobs in Michigan?
Migrate Mate filters job listings specifically by visa sponsorship availability, making it practical to search for research associate roles in Michigan without sorting through positions that don't support work authorization. You can narrow results by city, research discipline, and employer type. Michigan's university and healthcare sectors post regularly, so checking Migrate Mate frequently, particularly around academic hiring cycles in spring and fall, improves your chances of finding active openings.
Are there state-specific factors that affect visa sponsorship for research associates in Michigan?
Michigan's heavy reliance on university and hospital systems means many research associate positions are tied to grant funding, which can affect both hiring timelines and the duration of sponsorship. Employers must meet Department of Labor prevailing wage requirements for the relevant metropolitan statistical area, which differ between Ann Arbor, Detroit, and Grand Rapids. Research associates funded through federal grants at public universities may also encounter institutional policies that shape how and when sponsorship is initiated.
What is the prevailing wage for sponsored research associate jobs in Michigan?
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.