Top 27 research coordinator Jobs in michigan

Clinical Study Coordinator - CRI
University Pediatricians —Detroit, MI
- $48,000 - $52,000 a year
- Full-time
- Customer service
- HIPAA
- Mid-level
- Health savings account
- Health insurance
Quick Apply
Clinical Trial Coordinator
Oakland Hills Dermatology PC —Auburn Hills, MI
- From $20 an hour
- Full-time
- Microsoft Excel
- HIPAA
- Clinic experience
- Health insurance
- Dental insurance
Quick Apply
Clinical Data Coordinator
The START Center for Cancer Research —Grand Rapids, MI
- From $22 an hour
- Full-time
- Mid-level
- Bachelor's degree
- Experience equivalent to degree accepted
- Health savings account
- Disability insurance
Quick Apply
7d
DUA & Research Data Resources Coordinator
University of Michigan —Ann Arbor, MI
- Full-time
- Remote
- Background check
- Google Workspace
- Microsoft Outlook
- Health insurance
- Dental insurance
Clinical Research Coordinator - Department of Internal Medicine
Wayne State University —Detroit, MI
- $56,131 - $67,354 a year
- Full-time
- Background check
- Microsoft Excel
- Patient monitoring
Research Study Coordinator II, CCTRO New Trial Intake Coordinator) - Days - 40 Hours
Henry Ford Health —Detroit, MI
- Full-time
- Mid-level
- Bachelor's degree
- Home Health
- Health insurance
- Dental insurance
12d
Data Coordinator - Part-Time - Variable
Henry Ford Health —Jackson, MI
- Part-time
- Computer literacy
- Mid-level
- Office
- Health insurance
- Dental insurance
Assistant Clinical Research Coordinator- Cardiology/Neurology (Detroit, MI)
Profound Research —Detroit, MI
- Full-time
- Vital signs
- High school diploma or GED
- Clinic
- Health insurance
- Paid time off
Quick Apply
Clinical Research Coordinator II
Barbara Ann Karmanos Cancer Cn —Detroit, MI
- Full-time
- Surgery
- System design
- Mid-level
Clinical Research Coordinator Assistant - 1 YR Term Limited
University of Michigan —Ann Arbor, MI
- Full-time
- Microsoft Word
- Background check
- Psychiatry
- Health insurance
- Dental insurance
International Medical Graduate (IMG) - Clinical Research Coordinator
Revival Research Institute, LLC —Southfield, MI
- Full-time
- Medicine
- Microsoft Excel
- Microsoft Outlook
Quick Apply
Clinical Research Coord Assoc
University of Michigan —Ann Arbor, MI
- Full-time
- Background check
- Mid-level
- University
- Health insurance
- Dental insurance
Clinical Research Coordinator- Neurology (Detroit, MI)
Profound Research —Detroit, MI
- Full-time
- Patient monitoring
- Mid-level
- High school diploma or GED
- Health insurance
- Paid time off
Quick Apply
Clinical Research Coord Inter
University of Michigan —Ann Arbor, MI
- 8 hour shift
- Background check
- University
- Continuous improvement
- Health insurance
- Dental insurance
Clinical Research Coordinator
The Cancer & Hematology Centers —Grand Rapids, MI
- Full-time
- Mid-level
- Bachelor's degree
- Continuous improvement
Quick Apply
1d
Contractor- Assistant Clinical Research Coordinator (Detroit, MI)
Profound Research —Detroit, MI
- Full-time
- Vital signs
- Urgent Care
- Clinic experience
- Health insurance
- Paid time off
Quick Apply
1d
Coordinator Clinical Research
McLaren Health Care Corp —Flint, MI
- Full-time
- Surgery
- Mid-level
- High school diploma or GED
Clinical Research Coord Assoc (Term Limited)
University of Michigan —Ann Arbor, MI
- Full-time
- Hybrid work
- Background check
- Mid-level
- Databases
Research Study Coordinator I- Full time -Biorepository Research
Henry Ford Health —Detroit, MI
- Full-time
- Clinic
- Bachelor's degree
- Home Health
- Health insurance
- Dental insurance
6d
Facility Coordinator II, Division of Research & Innovation
Wayne State University —Detroit, MI
- $51,274 - $58,113 a year
- Full-time
- Background check
- Mid-level
- Office
8d

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Clinical Study Coordinator - CRI

University Pediatricians -
Detroit, MI

Quick Apply

Job Details

Full-time
$48,000 - $52,000 a year

Benefits

Health savings account
Health insurance
Dental insurance
401(k)
Flexible spending account
Tuition reimbursement
Paid time off
Employee assistance program
Vision insurance
401(k) matching
Life insurance

Qualifications

Project team coordination
Web-based survey tools
Clinical research
Customer service
Team leadership
Scientific research
HIPAA
Administrative experience
Bachelor's degree
Clinical data entry
Scientific protocols
Leading team collaboration initiatives
Implementing research protocols
Managing projects
Research and development project management
Quality data entry

Full Job Description

POSITION ANNOUNCEMENT

Position Title: Clinical Study Coordinator

Type: Hourly/Salary Non-exempt

Employment Status: Full-time

Salary: COMMENSURATE WITH EXPERIENECE

Date Requested: May 15, 2026

Available: IMMEDIATE

Position Purpose:

The Study Coordinator (SC) is a research professional who works alongside physicians, research nurses, study support staff, regulatory offices and staff, project sponsors, and Central Michigan University (CMU)/ University Pediatricians (UPeds) Clinical Research Center staff as it directly correlates to clinical trial studies. The SC will facilitate and coordinate clinical trial studies by performing these duties, in conjunction, with the principal investigator, institution, and funding organization. The SC will also submit regulatory (IRB) applications, hospital required compliance applications, and manage regulatory binders. In doing so, the study coordinator will provide support and guidance on the authority of compliance, financial, and other related aspects of the clinical study.

The CMU/UP Clinical Research Institute (CRI) is looking to fill the position of Research Study Coordinator. The candidate will work closely with research physicians and CRI staff to coordinate clinical research trials at the Children’s Hospital of Michigan. It is preferred that the candidate have research experience including patient consent and enrollment, clinical research study coordination, data and regulatory (IRB) management.

Qualifications:

Bachelor’s Degree required and one (1) year minimum experience in a related field. Familiarity with regulatory (IRB) applications and addressing issues. Three years experience conducting clinical trials and following study protocols. Data entry and familiarity with databases such as REDCap, OnCore, etc. Ability to draft and/or amend protocol study documents. Experience with Qualtrics and MS Suite. Experience in human subjects/health services research. Experience working in a multi-disciplinary team; demonstrated ability to take the lead on a projects, work independently, and following up with stakeholders. Experience in obtaining and processing samples. Must be detail oriented with strong communication and customer service skills. Knowledge and experience with clinical trial management systems Understanding of GCP and HIPAA rules and regulations. Exceptional leadership, organizational and communication skills.

Additional Desired Qualifications

1. Masters-level/ advanced degree with five (5) years experience managing clinical trials.

2. Relevant experience in an academic health center, medical school or higher education.

3. Certification as a Clinical Research Coordinator.

4. Clinical Trial Management System experience.

5. Experience with scientific writing literature searches (e.g., PubMed, Google Scholar) and EndNote, and communicating scientifically about research findings.

Certificates, Licenses, Registrations: None

Expectations and Responsibilities:

1. Serve as the primary coordinator for multiple protocols across disciplines. This includes managing the regulatory and operational aspects of the respective studies.

2. Assist the CMU-UP Clinical Research Institute in the start-up and development of a clinical trial management system – CTA (Oncore). This position will assist the CRI Executive Director and CRI pre- and post- award staff in the creation of the fields and processes related to the key tracking elements associated with research at CMU.

3. Assist with the preparation and maintenance of study files

4. Assist the Associate Director and Executive Director with internal audits of study binders, study files, and databases.

5. Responsible for the pulling of reports and auditing data entered the clinical trial management system.

6. Management of clinical trials for FDA investigational devices and drugs.

a. Patient consent and enrollment, patient follow-up, data collection and reporting and sponsor monitor visits.

b. Preparation of IRB documents for industry sponsored trials including new study submissions, continuations, amendments, unexpected events and closures. Maintaining regulatory binders and tracking.

c. Assist investigators with FDA submissions and IRB requirements of Compassionate Treatments.

d. Participation in site initiation and sponsor monitoring visits with CRI staff and Principal Investigators as needed.

e. Preparation of source documents for clinical trials. Update files as needed.

f. Study maintenance and preparation of study enrollment reports as requested.

Competencies

Customer Service - Respond promptly to customer needs; Responds to requests for service and assistance.

Interpersonal Skills - Maintain confidentiality; Listen to others without interrupting; Keep emotions under control; Remain open to others' ideas and tries new things.

Oral Communication - Speak clearly and persuasively in positive or negative situations; Participates in meetings.

Written Communication - Write clearly and informatively; Able to read and interpret written information.

Teamwork - Contribute to building a positive team spirit.

Ethics - Treat people with respect; Uphold organizational values.

Organizational Support - Follow policies and procedures, complete administrative tasks correctly and on time, support organization's goals and values.

Planning/Organizing - Organize or schedule other people and their tasks.

Quantity - Meet productivity standards.

Attendance/Punctuality - Is consistently at work and on time; ensure work responsibilities are covered when absent; arrive at meetings and appointments on time.

Working Conditions:

1. Regularly lift up to 25-50 pounds with or without assistance.

2. Able to complete duties under stress, deadlines, and while attending to multiple duties simultaneously.

3. Prolonged computer related exposure, as well as sitting and standing at workstations for long periods of time.

4. Noise level in the work environment is usually moderate.

5. Bending, sitting, walking, and standing frequently throughout the day.

6. Frequently work non-traditional hours as needed.

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Job Type: Full-time

Pay: $48,000.00 - $52,000.00 per year

Benefits:

401(k)
401(k) matching
Dental insurance
Employee assistance program
Flexible spending account
Health insurance
Health savings account
Life insurance
Paid time off
Tuition reimbursement
Vision insurance

Ability to Commute:

Detroit, MI 48201 (Required)

Ability to Relocate:

Detroit, MI 48201: Relocate before starting work (Required)

Work Location: In person

Quick Apply

Refine Your Search

research coordinator jobs in michigan

Clinical Study Coordinator - CRI

Clinical Trial Coordinator

Clinical Data Coordinator

DUA & Research Data Resources Coordinator

Clinical Research Coordinator - Department of Internal Medicine

Research Study Coordinator II, CCTRO New Trial Intake Coordinator) - Days - 40 Hours

Data Coordinator - Part-Time - Variable

Assistant Clinical Research Coordinator- Cardiology/Neurology (Detroit, MI)

Clinical Research Coordinator II

Clinical Research Coordinator Assistant - 1 YR Term Limited

International Medical Graduate (IMG) - Clinical Research Coordinator

Clinical Research Coord Assoc

Clinical Research Coordinator- Neurology (Detroit, MI)

Clinical Research Coord Inter

Clinical Research Coordinator

Contractor- Assistant Clinical Research Coordinator (Detroit, MI)

Coordinator Clinical Research

Clinical Research Coord Assoc (Term Limited)

Research Study Coordinator I- Full time -Biorepository Research

Facility Coordinator II, Division of Research & Innovation

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