Clinical Research Associate Jobs in Detroit, MI
Clinical Research Associate jobs in Detroit are concentrated in the Midtown Medical District, New Center, and the greater Detroit Medical Center corridor, with demand anchored in hospital networks, pharmaceutical services, and contract research organizations. Employers hiring right now include Profound Research, Wayne State University, and AbbVie. Scan the live roles below and apply to whichever ones fit.
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Showing 5 of 39+ Clinical Research Associate jobs
About Profound Research
- Compassion: We prioritize the patient-physician relationship, ensuring every interaction is service-oriented and patient-centered.
- Urgency: We work hard and practice selflessness, acting swiftly and decisively to meet the needs of our patients, partners, and colleagues.
- Solution Orientation: We embrace challenges with a positive mindset, communicate directly, and identify and implement effective solutions with efficiency.
- Excellence: We insist on excellence, holding ourselves accountable and empowering each other to deliver best-in-class service while maintaining the highest ethical and scientific standards.
- Conduct and manage all clinical trial activities in accordance with established research protocols and standards in compliance with all applicable laws, regulations, policies, and procedural requirements.
- Complete all relevant Profound Research required training, including but not limited to ICH-GCP certification and IATA certification in a timely manner.
- Mentor and train staff in the conduct of clinical trials, protocol requirements, communication and trial management skills.
- Lead, implement and coordinate duties for assigned clinical trials including but not limited to study start up, vendor management, subject recruitment, source document review and completion, protocol training, collection of regulatory documents, participant visits, timely data collection and documentation, management and reporting of adverse events, serious adverse events, and deviations, and monitoring visits and follow up.
- Ensure good documentation practices are applied by all team members when collecting, maintaining and correcting study data and required records of clinical trial activity including but not limited to source documentation, case report forms, queries, drug dispensation records, and regulatory forms.
- Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors.
- Collect and account for supplies from sponsors such as lab kits, ancillary supplies, and investigational products.
- Other duties as assigned.
- Bachelor’s degree and 2 years relevant experience in the life science industry OR
- Associate’s degree with 4 years relevant experience in the life science industry OR
- High School Graduate and/or technical degree with minimum of 6 years relevant experience in the life science industry AND 1 year
- Clinical Research Coordinator experience
- Successful completion of GCP certification and Certified Clinical Research Coordinator (CCRC) certification within 6 months of being in the role
- Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens
- Proficient ability to work independently, plan and prioritize with minimal guidance
- Excellent attention to detail, organization, and communication with varied stakeholders
- Ability to work as a team player with the ability to adapt to changing schedules and assignments
Physical Requirements & Work Environment
- This role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
- Requires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
- Must be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
- May be required to wear personal protective equipment (PPE) in accordance with facility protocols
- Travel between company sites, meetings, or partner locations may be required
- Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
Why Join Profound Research?
- Meaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters
- Professional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
- Leadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
- Collaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
- Full Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
- Diverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
About Profound Research
- Compassion: We prioritize the patient-physician relationship, ensuring every interaction is service-oriented and patient-centered.
- Urgency: We work hard and practice selflessness, acting swiftly and decisively to meet the needs of our patients, partners, and colleagues.
- Solution Orientation: We embrace challenges with a positive mindset, communicate directly, and identify and implement effective solutions with efficiency.
- Excellence: We insist on excellence, holding ourselves accountable and empowering each other to deliver best-in-class service while maintaining the highest ethical and scientific standards.
- Conduct and manage all clinical trial activities in accordance with established research protocols and standards in compliance with all applicable laws, regulations, policies, and procedural requirements.
- Complete all relevant Profound Research required training, including but not limited to ICH-GCP certification and IATA certification in a timely manner.
- Mentor and train staff in the conduct of clinical trials, protocol requirements, communication and trial management skills.
- Lead, implement and coordinate duties for assigned clinical trials including but not limited to study start up, vendor management, subject recruitment, source document review and completion, protocol training, collection of regulatory documents, participant visits, timely data collection and documentation, management and reporting of adverse events, serious adverse events, and deviations, and monitoring visits and follow up.
- Ensure good documentation practices are applied by all team members when collecting, maintaining and correcting study data and required records of clinical trial activity including but not limited to source documentation, case report forms, queries, drug dispensation records, and regulatory forms.
- Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors.
- Collect and account for supplies from sponsors such as lab kits, ancillary supplies, and investigational products.
- Other duties as assigned.
- Bachelor’s degree and 2 years relevant experience in the life science industry OR
- Associate’s degree with 4 years relevant experience in the life science industry OR
- High School Graduate and/or technical degree with minimum of 6 years relevant experience in the life science industry AND 1 year
- Clinical Research Coordinator experience
- Successful completion of GCP certification and Certified Clinical Research Coordinator (CCRC) certification within 6 months of being in the role
- Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens
- Proficient ability to work independently, plan and prioritize with minimal guidance
- Excellent attention to detail, organization, and communication with varied stakeholders
- Ability to work as a team player with the ability to adapt to changing schedules and assignments
Physical Requirements & Work Environment
- This role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
- Requires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
- Must be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
- May be required to wear personal protective equipment (PPE) in accordance with facility protocols
- Travel between company sites, meetings, or partner locations may be required
- Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
Why Join Profound Research?
- Meaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters
- Professional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
- Leadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
- Collaborative Culture: You’ll work alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
- Full Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
- Diverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
See All 39 Clinical Research Associate Jobs in Detroit
Find roles in Detroit that match your experience and apply in just a few clicks.
Find JobsClinical Research Associate Job Market in Detroit
Who's Hiring
- Profound Research11
- Wayne State University7
- AbbVie4
- Eccalon4
- Science 374
Top Industries Hiring
- Education
- Healthcare & Medical Services
Clinical Research Associate Jobs in Detroit: Frequently Asked Questions
How do I get a clinical research associate job in Detroit?
Focus your search on Detroit's Midtown Medical District, the Detroit Medical Center campus, and the New Center area, where hospital systems, contract research organizations, and pharmaceutical affiliates cluster most of their clinical operations. Candidates with hands-on protocol management experience and GCP certification move fastest in this market. Familiarity with oncology, cardiology, or neurology trials gives a meaningful edge given the specialties that drive trial volume locally.
Which companies hire clinical research associates in Detroit?
Employers hiring clinical research associates in Detroit right now include Profound Research, Wayne State University, and AbbVie, based on current listings on Migrate Mate as of September 2026. Detroit's hiring mix includes large academic medical centers, regional hospital networks, and contract research organizations with site-based operations tied to the city's dense concentration of teaching hospitals.
Are there remote clinical research associate jobs in Detroit?
Yes, but with limits: clinical research associate work is heavily site-based by nature, so fully remote roles are less common than in purely desk-based fields. About 53% of clinical research associate openings tied to Detroit are remote or hybrid as of September 2026, with remote work most available for data review, regulatory document management, and sponsor-side monitoring roles rather than on-site patient-facing coordination.
How can I get a clinical research associate job in Detroit with little or no experience?
The most realistic entry path in Detroit is through a clinical research coordinator or research assistant role at one of the city's academic medical centers or large hospital networks, which regularly hire candidates with a life sciences degree and lab or patient-facing experience. Detroit's robust teaching hospital ecosystem means entry-level research staff openings appear regularly, and moving into a clinical research associate role after one to two years of site coordination experience is a well-established local progression.
Which industries hire the most clinical research associates in Detroit?
Detroit clinical research associate roles concentrate in Education and Healthcare & Medical Services, based on current listings on Migrate Mate as of September 2026. Detroit's strong academic medical infrastructure and its ties to regional pharmaceutical and biotech operations make healthcare systems and contract research the dominant sources of local hiring for this role.
See All 39 Clinical Research Associate Jobs in Detroit
Find roles in Detroit that match your experience and apply in just a few clicks.
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