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Research Monitor Jobs in Michigan (NOW HIRING)

Imh

Clinical Research Assistant

Almont, MI · On-site

$19.50 - $26.48/hr

Archives research study records at study closure. * Scheduling & Inventory Management ... Schedule monitoring and vendor visits and manage study kit inventory. * Prescreening Activities ...

THOMSON REUTERS

Research Engineer

Ann Arbor, MI · Hybrid

We are seeking a Research Engineer who willbringexpertiseinAI and ML andisinterestedinbuilding data ... Proficiencyin automation, system monitoring, and cloud-native applications, with familiarity in AWS ...

A.P.R., Inc. (AlphaProTemps)

Be Seen First

Clinical Research Coordinator (CRC)

Kalamazoo, MI · On-site

$44/hr

Prepare, submit, and monitor documentation for research programs. * Ensure compliance with research regulations and protocols through audits. * Advise caregivers on program design, treatment ...

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Research Monitor information

What is the difference between Research Monitor vs Research Analyst?

AspectResearch MonitorResearch Analyst
Required CredentialsBachelor's degree in related field; certifications optionalBachelor's or master's degree in related field; certifications beneficial
Work EnvironmentMonitoring research activities, ensuring compliance, overseeing data collectionAnalyzing data, preparing reports, interpreting research findings
Employer & Industry UsageResearch institutions, market research firms, academic settingsMarket research firms, financial institutions, consulting firms

Research Monitors primarily oversee research processes and ensure compliance, while Research Analysts focus on analyzing data and producing insights. Both roles require similar educational backgrounds, but their responsibilities differ significantly within the research process.

What are some common challenges faced by research monitors when overseeing clinical trials?

Research Monitors often encounter challenges such as ensuring consistent adherence to protocols across multiple sites, managing complex regulatory documentation, and effectively communicating findings to both site staff and sponsors. They must be detail-oriented to identify potential issues in data collection and patient safety while balancing frequent travel and tight timelines. Building strong relationships with site teams and staying current with regulatory changes can help address these challenges and contribute to the success of clinical trials.

What are the key skills and qualifications needed to thrive as a research monitor, and why are they important?

To thrive as a Research Monitor, you need a strong understanding of research ethics, regulatory compliance, and clinical trial protocols, often supported by a degree in a health or science field. Familiarity with data management systems, electronic case report forms (eCRFs), and Good Clinical Practice (GCP) certification is typically required. Attention to detail, strong organizational skills, and effective communication are crucial soft skills for ensuring research integrity and clear reporting. These skills ensure that studies comply with regulations, data is accurate, and participant safety is maintained throughout the research process.

What is a research monitor?

Research Monitors are professionals responsible for overseeing the conduct of research studies to ensure compliance with protocols, regulations, and ethical standards. They play a crucial role in monitoring clinical trials or other research projects by reviewing data, conducting site visits, and verifying that procedures are followed correctly. Research Monitors help protect the integrity of the research and the safety of participants by identifying and addressing any issues that arise during the study. Their work ensures that research results are reliable and that all activities adhere to established guidelines.

How to become a research monitor?

To become a research monitor, candidates typically need a bachelor's degree in a relevant field such as health sciences, social sciences, or research methodology. Experience with data collection, analysis, and familiarity with research protocols or software like SPSS or SAS can be beneficial. Certifications in research ethics or project management may also enhance prospects.

How much does a research monitor make?

Research monitors typically earn between $50,000 and $80,000 annually, depending on experience, location, and the industry they work in. Entry-level positions may start lower, while experienced professionals with specialized skills can earn higher salaries. Many roles also offer benefits such as health insurance and flexible schedules.
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Research Monitor jobs near you
Infographic showing various Research Monitor job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 13% Part Time, 2% Temporary, 5% Contract, and 1% Nights. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution.

Coordinator Clinical Research

McLaren Health Care Corp

Flint, MI • On-site

$23.50 - $31.25/hr

Full-time

Re-posted 24 days ago

McLaren Health Care rating

6.7

Company rating: 6.7 out of 10

Based on 221 frontline employees who took The Breakroom Quiz

531st of 887 rated healthcare providers

Job description

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:

1.      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.

2.      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.

3.      Registers and randomizes eligible patients.

4.      Submits accurately completed data collection forms to the sponsor or CRO in a timely manner as dictated by the study protocol.

5.      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.

6.      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.

7.      Assists the investigators and clinicians in identifying and enrolling eligible patients into clinical trials/ studies and assures compliance to protocol requirements.

8.      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:

  • High School Diploma or equivalent
  • Two years' experience in clinical research or five-years in a health care role (ex. paramedic, emergency medical technician, radiology technician) 

Preferred: 

  • Degree in biology, psychology, or other clinical research -related area or equivalent education and experience
  • Three or more years of experience in clinical research
  • Clinical research certification through SOCRA or ACRP

Equal Opportunity Employer of Minorities/Females/Disabled/Veterans

Additional Information
  • Schedule: Full-time
  • Requisition ID: 26002728
  • Daily Work Times: 8am - 4:30pm
  • Hours Per Pay Period: 80
  • On Call: No
  • Weekends: No

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