Coordinator Clinical Research
Michigan, MIFull-timeSeen 3w agoSeen in employer's feed 6 days ago
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At a glance
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Job overview
The Clinical Research Coordinator facilitates research studies and provides protocol information to medical and nursing staff. The role evaluates candidate eligibility, assists with informed consent, registers and randomizes eligible patients, and coordinates study procedures. It also supports protocol compliance, data collection and submission, regulatory documentation, and patient and family education about research protocols and study changes.
Skills & qualifications
Skills
Qualifications
Full job description
Coordinator Clinical Research
Michigan, Flint (https://careers.mclaren.org/jobs/38924/other-jobs-matching/location-only)
Health Professional
McLaren Health Care Corp
26010879 Requisition #
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Position Summary:
Responsible for facilitating research studies; providing knowledgeable information regarding each research protocol to the medical and nursing staff; evaluating the eligibility of potential candidates for research studies; assisting in the informed consent process; monitoring research study compliance; collecting and submitting data; coordinating required study procedures to meet protocol requirements and maintain a system for effective data flow.
Essential Functions and Responsibilities :
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Evaluates eligibility of candidates for clinical research studies by reviewing protocol defined eligibility requirements and/or collecting pertinent data on potential candidates, verifying appropriateness of patients for entry to clinical trials, and assisting the other staff in determining eligibility of potential patients.
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Assists the investigator with the informed consent process and assures that the research team and the patient have adequate information to achieve the informed consent process.
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Registers and randomizes eligible patients.
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Submits accurately completed data collection forms to the sponsor or CRO in a timely manner as dictated by the study protocol.
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Coordinates tests and procedures as specified in the study protocol through accurate communication with the site / principal investigator, physicians, patients, nurses, and office/hospital staff.
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Maintains contact with regulatory specialist to ensure data submitted to the IRB of record is accurate and timely. Upon request, submits regulatory documents to regulatory specialist to include in the IRB submission or submission to sponsor or CRO.
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Assists the investigators and clinicians in identifying and enrolling eligible patients into clinical trials/ studies and assures compliance to protocol requirements.
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Educates patients and their families regarding research protocols and keeps them informed of procedures and changes in the studies in which they are participating.
Qualifications :
Required:
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High School Diploma or equivalent
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Two years’ experience in clinical research or five-years in a health care role (ex. paramedic, emergency medical technician, radiology technician)
Preferred:
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Degree in biology, psychology, or other clinical research -related area or equivalent education and experience
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Three or more years of experience in clinical research
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Clinical research certification through SOCRA or ACRP
Equal Opportunity Employer of Minorities/Females/Disabled/Veterans
Additional Information
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Schedule: Full-time
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Requisition ID: 26010879
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Daily Work Times: 8am - 4:30pm
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Hours Per Pay Period: 80
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On Call: No
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Weekends: No
How this job compares
Set against the 609 open Clinical Research Coordinator jobs on Olive Jobs, counted November 4, 2026.
- Pay
- This postingNot listed
- US median$57–74K/yr154 salary ranges
- US median$24–36/hr179 hourly ranges
- Openings
- Olive Jobs lists 21 open Clinical Research Coordinator jobs in Michigan and 609 across the US. 2% of them nationwide are listed as remote or flexible.
- Hiring the most in Michigan
- University of Michigan12 open
- McLaren Health Care (this employer)3 open
- IQVIA2 open
- Experience
- This posting asks for at least 2 years of experience; Clinical Research Coordinator postings that state a minimum ask for 2 years at the median (399 postings).
- Education
- 191 of the 609 open Clinical Research Coordinator jobs (31%) ask for a bachelor's degree or higher.
Counted across the open, public US postings on Olive Jobs on November 4, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.
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