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Clinical Research Coordinator II- MT Pleasant, MI

McLaren Health Care

Michigan, MIFull-timeSeen 6 days agoSeen in employer's feed today

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At a glance

Compensation
No compensation found
Location
Michigan, MI
Schedule
Full-time
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Job overview

The Clinical Research Coordinator II provides study coordination, data management, and regulatory support to the Clinical Trials Office. The coordinator manages independent assignments and provides customer support and guidance in the clinical trials arena.

Skills & qualifications

RequiredNice to have

Skills

Study CoordinationData ManagementRegulatory SupportClinical Trials

Qualifications

Bachelor's Degree or EquivalentMedical or Science Experience or EducationClinical Research Certification

Full job description

Clinical Research Coordinator II- MT Pleasant, MI

Michigan, Flint (https://careers.mclaren.org/jobs/39445/other-jobs-matching/location-only)

Non-Health Professional

Barbara Ann Karmanos Cancer In

26011511 Requisition #

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Location: Mt Pleasant, Michigan

Karmanos Cancer Institute at McLaren Central Michigan

1221 South Drive

Mt. Pleasant, MI 48858

Job Summary:Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent customer support and guidance in the clinical trials arena.

Responsibilities:

  • Assure all study requirements are met and documented and meet both internal and external regulations in accordance with protocol guidelines.

  • Maintain logs, including tracker submissions and update the CTO Oncore database in a timely manner according to CTO SOPs.

  • Design systems for coordinating, compiling and submission of data; design workflow processes and participate in quality assurance measures; coordinate site visits.

  • Manage all patient and/or protocol data as assigned and respond to queries in a timely fashion.

  • Schedule and participate in monitoring visits and participate in multidisciplinary team program meetings as required.

Qualifications:

  • Bachelor’s degree required or equivalent combination of education and experience.

  • Medical and/or science experience/education preferred.

  • Clinical research certification preferred.

Equal Opportunity Employer of Minorities/Females/Disabled/Veterans

Additional Information

  • Schedule: Full-time

  • Requisition ID: 26011511

  • Daily Work Times: 8:00am-4:30pm

  • Hours Per Pay Period: 80

  • On Call: No

  • 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
Experience
Clinical Research Coordinator postings that state a minimum ask for 2 years of experience at the median; the middle half ask for 1 to 3 years (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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