Clinical Research Visa Sponsorship Jobs in Michigan
Michigan's clinical research sector is anchored by major health systems and research universities, including the University of Michigan Health System in Ann Arbor, Henry Ford Health in Detroit, and Spectrum Health in Grand Rapids. Employers in this field regularly sponsor H-1B visa and J-1 visas for qualified international candidates in clinical research coordinator, associate, and scientist roles.
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Get Access To All JobsMission Statement
Michigan Medicine improves the health of patients, populations and communities through excellence in education, patient care, community service, research and technology development, and through leadership activities in Michigan, nationally and internationally. Our mission is guided by our Strategic Principles and has three critical components; patient care, education and research that together enhance our contribution to society.
Job Summary
The REMEDY team at the University of Michigan (UM) manages the vast portfolio of surgical clinical trials for the Department of Cardiac Surgery. The team consists of varying levels of coordinators dedicated to advancing healthcare to improve outcomes for patients. Our collaborators include investigators from other departments within UM, industries, and Universities. We specialize in multi-center, including international, device trials as well as outcomes research, drug trials, and investigator-initiated studies. As we continue to expand our portfolio, we are looking for detail orientated, highly motivated, compassionate individuals to join our team.
This clinical research coordinator (CRC) position may provide study coordination for multiple clinical research studies depending on complexity that range from moderate to complex. Coordinator experience and mastery of all job duties from the CRC-Technician position on the Michigan Medicine CRC Career Ladder is required. This position should be able to perform tasks and make decisions independently, consistently, and accurately, and demonstrate that they have achieved a moderate level of expertise in all their skills and abilities resulting in high quality work. It is presumed that this position is able to apply their skills to a broad range of different types of clinical studies, navigate available resources appropriately, effectively use all tools and job aids at their disposal and operate e-clinical technologies with a reasonable degree of proficiency. This position can perform the majority of tasks independently and perform quality checks of their work. They also know where and how to identify appropriate resources and support and are able to discern when to escalate issues needing additional intervention. Key behavioral competency descriptors include demonstrate, implement, execute, and use.
Responsibilities
Independent knowledge, skills, and abilities within all 8 competency domains is expected:
- Scientific Concepts and Research Design
- Ethical Participant Safety Considerations
- Investigational Products Development and Regulation
- Clinical Study Operations (GCPs)
- Study and Site Management
- Data Management and Informatics
- Leadership and Professionalism
- Communication and Teamwork
Responsibilities will include, but are not limited to:
- Understanding of protocol elements/requirements
- Executing study procedures
- Anticipating and mitigating the potential for protocol non-compliance
- Accurate implementation of protocol procedures
- Describing and performing routine study management activities
- Performing study procedures with minimal supervision
- Triaging routine participant concerns and issues appropriately
- Scheduling, assisting with preparation, and attending study-related meetings (e.g. study initiation meetings, audits, monitoring visits, or community-based organizational meetings)
- Participating in regular study meetings
- Properly completing payment forms and pays participants accordingly
- Serving as primary point of contact for study and/or a study team
- Documenting data in accordance with ALCOA-C principles and/or the study data management plan
- Completing complex data collection during study visits
- Resolving data queries
- Appropriately identifying and reporting adverse events (AEs), Serious Adverse Events (SAEs), and Other Reportable Information and Occurrences (ORIOs)
- Maintaining essential documents as outlined in the GCP guidelines, or other relevant guidelines.
- Other related duties as assigned.
Supervision Received: This position reports directly to the Clinical Trial Lead for the Department of Cardiac Surgery.
Supervision Exercised: None.
Required Qualifications
- Bachelor's degree in Health Science or an equivalent combination of related education and experience is necessary.
- 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 prior to applying.)
- 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 for qualifying experience prior to applying.)
Desired Qualifications
- 4+ years of direct related experience
- 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.
Why Join Michigan Medicine?
Michigan Medicine is one of the largest health care complexes in the world and has been the site of many groundbreaking medical and technological advancements since the opening of the U-M Medical School in 1850. Michigan Medicine is comprised of over 30,000 employees and our vision is to attract, inspire, and develop outstanding people in medicine, sciences, and healthcare to become one of the world’s most distinguished academic health systems. In some way, great or small, every person here helps to advance this world-class institution. Work at Michigan Medicine and become a victor for the greater good.
What Benefits can you Look Forward to?
- Excellent medical, dental and vision coverage effective on your very first day
- 2:1 Match on retirement savings
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
Hours/Week: 40 hours
Shift/Hours/Days: Days, occasional evening and weekends, on call
Application Deadline
Job openings are posted for a minimum of seven calendar days. The review and selection process may begin as early as the eighth day after posting. This opening may be removed from posting boards and filled any time after the minimum posting period has ended.
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
282408
Working Title
Clinical Research Coord Assoc
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 Cardiac Surgery
Posting Begin/End Date
8/28/2026 - 9/11/2026
Career Interest
Research
Mission Statement
Michigan Medicine improves the health of patients, populations and communities through excellence in education, patient care, community service, research and technology development, and through leadership activities in Michigan, nationally and internationally. Our mission is guided by our Strategic Principles and has three critical components; patient care, education and research that together enhance our contribution to society.
Job Summary
The REMEDY team at the University of Michigan (UM) manages the vast portfolio of surgical clinical trials for the Department of Cardiac Surgery. The team consists of varying levels of coordinators dedicated to advancing healthcare to improve outcomes for patients. Our collaborators include investigators from other departments within UM, industries, and Universities. We specialize in multi-center, including international, device trials as well as outcomes research, drug trials, and investigator-initiated studies. As we continue to expand our portfolio, we are looking for detail orientated, highly motivated, compassionate individuals to join our team.
This clinical research coordinator (CRC) position may provide study coordination for multiple clinical research studies depending on complexity that range from moderate to complex. Coordinator experience and mastery of all job duties from the CRC-Technician position on the Michigan Medicine CRC Career Ladder is required. This position should be able to perform tasks and make decisions independently, consistently, and accurately, and demonstrate that they have achieved a moderate level of expertise in all their skills and abilities resulting in high quality work. It is presumed that this position is able to apply their skills to a broad range of different types of clinical studies, navigate available resources appropriately, effectively use all tools and job aids at their disposal and operate e-clinical technologies with a reasonable degree of proficiency. This position can perform the majority of tasks independently and perform quality checks of their work. They also know where and how to identify appropriate resources and support and are able to discern when to escalate issues needing additional intervention. Key behavioral competency descriptors include demonstrate, implement, execute, and use.
Responsibilities
Independent knowledge, skills, and abilities within all 8 competency domains is expected:
- Scientific Concepts and Research Design
- Ethical Participant Safety Considerations
- Investigational Products Development and Regulation
- Clinical Study Operations (GCPs)
- Study and Site Management
- Data Management and Informatics
- Leadership and Professionalism
- Communication and Teamwork
Responsibilities will include, but are not limited to:
- Understanding of protocol elements/requirements
- Executing study procedures
- Anticipating and mitigating the potential for protocol non-compliance
- Accurate implementation of protocol procedures
- Describing and performing routine study management activities
- Performing study procedures with minimal supervision
- Triaging routine participant concerns and issues appropriately
- Scheduling, assisting with preparation, and attending study-related meetings (e.g. study initiation meetings, audits, monitoring visits, or community-based organizational meetings)
- Participating in regular study meetings
- Properly completing payment forms and pays participants accordingly
- Serving as primary point of contact for study and/or a study team
- Documenting data in accordance with ALCOA-C principles and/or the study data management plan
- Completing complex data collection during study visits
- Resolving data queries
- Appropriately identifying and reporting adverse events (AEs), Serious Adverse Events (SAEs), and Other Reportable Information and Occurrences (ORIOs)
- Maintaining essential documents as outlined in the GCP guidelines, or other relevant guidelines.
- Other related duties as assigned.
Supervision Received: This position reports directly to the Clinical Trial Lead for the Department of Cardiac Surgery.
Supervision Exercised: None.
Required Qualifications
- Bachelor's degree in Health Science or an equivalent combination of related education and experience is necessary.
- 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 prior to applying.)
- 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 for qualifying experience prior to applying.)
Desired Qualifications
- 4+ years of direct related experience
- 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.
Why Join Michigan Medicine?
Michigan Medicine is one of the largest health care complexes in the world and has been the site of many groundbreaking medical and technological advancements since the opening of the U-M Medical School in 1850. Michigan Medicine is comprised of over 30,000 employees and our vision is to attract, inspire, and develop outstanding people in medicine, sciences, and healthcare to become one of the world’s most distinguished academic health systems. In some way, great or small, every person here helps to advance this world-class institution. Work at Michigan Medicine and become a victor for the greater good.
What Benefits can you Look Forward to?
- Excellent medical, dental and vision coverage effective on your very first day
- 2:1 Match on retirement savings
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
Hours/Week: 40 hours
Shift/Hours/Days: Days, occasional evening and weekends, on call
Application Deadline
Job openings are posted for a minimum of seven calendar days. The review and selection process may begin as early as the eighth day after posting. This opening may be removed from posting boards and filled any time after the minimum posting period has ended.
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
282408
Working Title
Clinical Research Coord Assoc
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 Cardiac Surgery
Posting Begin/End Date
8/28/2026 - 9/11/2026
Career Interest
Research
Clinical Research Job Roles in Michigan
See all 47+ Clinical Research Jobs in Michigan
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Search Clinical Research Jobs in MichiganClinical Research Jobs in Michigan: Frequently Asked Questions
Which companies sponsor visas for clinical research roles in Michigan?
Major sponsors for clinical research positions in Michigan include the University of Michigan, Michigan Medicine, Henry Ford Health System, Beaumont Health, Spectrum Health, and Kalamazoo-based pharmaceutical firms like Pfizer's Michigan operations and Perrigo. Academic medical centers and large hospital networks account for the majority of H-1B and J-1 sponsorships in this field across the state.
Which visa types are most common for clinical research roles in Michigan?
The H-1B is the most common work visa for clinical research coordinators, associates, and scientists in Michigan, as these roles typically require at least a bachelor's degree in a life science or health-related field. J-1 visas are also common, particularly for research scholars and postdoctoral fellows at institutions like the University of Michigan and Wayne State University.
Which cities in Michigan have the most clinical research sponsorship jobs?
Ann Arbor leads Michigan for clinical research sponsorship activity, driven by the University of Michigan's extensive research enterprise. Detroit and its surrounding metro area follows, anchored by Henry Ford Health, Wayne State University, and Beaumont Health. Grand Rapids is a growing hub, supported by Spectrum Health and the Van Andel Research Institute, which regularly hires international research staff.
How to find clinical research visa sponsorship jobs in Michigan?
Migrate Mate filters clinical research jobs in Michigan specifically by visa sponsorship, so you can see which employers are actively hiring international candidates rather than sifting through listings that don't sponsor. Search for roles like clinical research coordinator, clinical research associate, and research scientist on Migrate Mate and filter to Michigan to find relevant openings at health systems, universities, and CROs operating in the state.
Are there state-specific considerations for clinical research roles and visa sponsorship in Michigan?
Michigan's concentration of academic medical centers means many clinical research positions are tied to grant-funded projects, which can affect sponsorship timelines since funding cycles influence hiring windows. Candidates with backgrounds in oncology, cardiology, or neurology research are particularly in demand given the specialty focus of Michigan's major health systems. A relevant life science degree is generally required for H-1B sponsorship eligibility in this field.
What is the prevailing wage for sponsored clinical research 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.