Clinical Research Coordinator Jobs in Michigan
Clinical Research Coordinator jobs in Michigan are concentrated in the life sciences, health system research, and pharmaceutical sectors, with openings at every experience level from entry-level research assistant to senior coordinator overseeing multi-site trials. Detroit, Ann Arbor, and Grand Rapids account for the largest share of postings, anchored by employers like Henry Ford Health, University of Michigan Health, and the Karmanos Cancer Institute. Oncology trials, cardiovascular research, and sponsor-funded Phase II and III studies are the most in-demand specialties statewide. Scan the live roles below and apply to whichever ones fit.
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Showing 5 of 12+ Clinical Research Coordinator jobs
Novi, United States of America | Part time | Office-based | R1577430
Clinical Research Coordinator - Novi, MI
Work Set-Up: On-site
Schedule Weekly Hours: 24 hours/week
About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.
About the Role
We are seeking a Clinical Research Coordinator (CRC) to join our team and support clinical research studies under the supervision of a principal investigator. This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance.
Key Responsibilities
- Perform a variety of clinical procedures, including ECG, sample collection, and vital signs.
- Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.
- Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.
- Recruit, screen, and orient patients, ensuring their safety and well-being throughout the study.
- Collect and accurately record clinical data in case report forms (CRFs).
- Collaborate with investigators and monitors, addressing queries and ensuring data quality.
- Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.
Qualifications
- Bachelor’s degree preferred or equivalent combination of education and relevant experience.
- Minimum 1+ years of relevant work experience in clinical research.
- Working knowledge of clinical trials, GCP principles, and medical terminology.
- Experience with prescreening patients based on inclusionary/exclusionary criteria.
- Familiarity with patient chart/medical record review.
- Ability to support patient study visits.
- Strong attention to detail and ability to establish effective working relationships.
- Proficiency with EDC systems, data entry accuracy, and query management.
Please note: This position is not eligible for sponsorship.
#LI-CES #LI-DNP #LI-HCP
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.Where you'll work
Office-based
You’ll work primarily from one of our office locations, collaborating closely with colleagues in a dynamic, team-oriented environment. This setting offers access to on-site resources, real-time interaction and opportunities to build strong relationships through in-person work.
Culture
Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.
Novi, United States of America | Part time | Office-based | R1577430
Clinical Research Coordinator - Novi, MI
Work Set-Up: On-site
Schedule Weekly Hours: 24 hours/week
About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.
About the Role
We are seeking a Clinical Research Coordinator (CRC) to join our team and support clinical research studies under the supervision of a principal investigator. This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance.
Key Responsibilities
- Perform a variety of clinical procedures, including ECG, sample collection, and vital signs.
- Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.
- Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.
- Recruit, screen, and orient patients, ensuring their safety and well-being throughout the study.
- Collect and accurately record clinical data in case report forms (CRFs).
- Collaborate with investigators and monitors, addressing queries and ensuring data quality.
- Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.
Qualifications
- Bachelor’s degree preferred or equivalent combination of education and relevant experience.
- Minimum 1+ years of relevant work experience in clinical research.
- Working knowledge of clinical trials, GCP principles, and medical terminology.
- Experience with prescreening patients based on inclusionary/exclusionary criteria.
- Familiarity with patient chart/medical record review.
- Ability to support patient study visits.
- Strong attention to detail and ability to establish effective working relationships.
- Proficiency with EDC systems, data entry accuracy, and query management.
Please note: This position is not eligible for sponsorship.
#LI-CES #LI-DNP #LI-HCP
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.Where you'll work
Office-based
You’ll work primarily from one of our office locations, collaborating closely with colleagues in a dynamic, team-oriented environment. This setting offers access to on-site resources, real-time interaction and opportunities to build strong relationships through in-person work.
Culture
Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.
See All 12 Clinical Research Coordinator Jobs in Michigan
Find roles in Michigan that match your experience and apply in just a few clicks.
Find JobsClinical Research Coordinator Jobs by City in Michigan
Where Michigan roles are concentrated, by current openings.
Clinical Research Coordinator Job Market in Michigan
A snapshot from current Michigan openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Education
- Healthcare & Medical Services
What Michigan Employers Look For
The qualifications that appear most often in clinical research coordinator jobs across Michigan.
- Bachelor's degree in life sciences, nursing, public health, or a related clinical field
- ACRP or SOCRA certification (CCRC or CCRP) preferred or required by most Michigan health systems
- Minimum two years of clinical trials or direct patient-contact research experience
- Working knowledge of FDA regulations, ICH-GCP guidelines, and IRB submission processes
- Proficiency with clinical trial management systems such as Medidata Rave or Oracle Inform
- Strong source document verification skills and experience maintaining regulatory binders
Clinical Research Coordinator Jobs in Michigan: Frequently Asked Questions
How do you become a clinical research coordinator in Michigan?
Most Michigan employers require a bachelor's degree in a life science, nursing, or health-related field as the starting point. Michigan does not issue a state-specific license for clinical research coordinators, so the credential that carries the most weight is national certification through ACRP (the CCRC credential) or SOCRA (the CCRP credential). Both require documented clinical research experience and a passing exam score. Large Michigan health systems such as the University of Michigan and Spectrum Health commonly list one of these certifications as preferred for coordinator roles.
How much do clinical research coordinators make in Michigan?
Clinical research coordinators in Michigan earn a median of about $129,070 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $68,380 for the lowest 10% to over $222,030 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire clinical research coordinators in Michigan?
Companies currently hiring clinical research coordinators in Michigan include IQVIA, Iterative Health, and McLaren Health Care, per current listings on Migrate Mate as of November 2026. Michigan's concentration of academic medical centers, cancer institutes, and contract research organizations means demand is spread across health systems, specialty clinics, and CRO field offices throughout the state.
Which Michigan cities have the most clinical research coordinator jobs?
Detroit, Novi, and Troy consistently lead Michigan for clinical research coordinator openings. Ann Arbor's concentration is driven by the University of Michigan Health system and its affiliated research institutes, while Detroit's volume reflects the density of large health systems including Henry Ford Health and the Karmanos Cancer Institute, and Grand Rapids has grown as a hub through Corewell Health's expanding research infrastructure.
Are there remote clinical research coordinator jobs in Michigan?
Yes, but they're limited. Clinical research coordinators spend a meaningful portion of their time on-site conducting patient visits, collecting specimens, and maintaining source documents, which keeps most roles tied to a facility. About 0% of clinical research coordinator openings tied to Michigan are remote or hybrid as of November 2026, and the roles most likely to offer flexibility are those focused on data entry, regulatory document management, or monitoring for sponsor-side or CRO positions.
How can I get hired as a clinical research coordinator in Michigan with little or no experience?
The most realistic entry path is moving into a research assistant or clinical research associate role at a Michigan academic medical center, then building toward coordinator responsibilities. The University of Michigan, Michigan Medicine, and Henry Ford Health regularly post research assistant and coordinator-in-training positions that do not require prior trials experience. Adjacent roles like medical assistant, phlebotomist, or EMT that involve direct patient contact are common stepping stones. Earning your IATA or GCP training certificate before applying, and volunteering through a university's IRB office, signals commitment and gives a candidate a concrete edge.
Where can I find and apply to clinical research coordinator jobs in Michigan?
You can find and apply to clinical research coordinator jobs in Michigan on Migrate Mate, which lists current Michigan openings. Search the available roles, find the ones that match your experience and location, and apply directly to the ones that fit.
See All 12 Clinical Research Coordinator Jobs in Michigan
Find roles in Michigan that match your experience and apply in just a few clicks.
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