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Clinical Research Study Assistant Jobs in Michigan

McLaren

Coordinator Clinical Research

Flint, MI · On-site

$23.50 - $31.25/hr

Responsible for facilitating research studies; providing knowledgeable information regarding each research protocol to the medical and nursing staff; evaluating the eligibility of potential ...

Imh

Clinical Research Assistant

Almont, MI · On-site

$19.50 - $26.48/hr

... to assist in duties and activities associated with supporting clinical research and research ... Archives research study records at study closure. * Scheduling & Inventory Management : Schedule ...

Insight

Clinical Research Assistant

Flint, MI

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Clinical Research Assistant will support the clinical research team at our Research Dearborn ... Ability and willingness to commute between our research locations as needed per study tasks

Insight

Clinical Research Assistant

Flint, MI · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Clinical Research Assistant will support the clinical research team at our Research Dearborn ... Ability and willingness to commute between our research locations as needed per study tasks

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All JobsClinical Research Study JobsClinical Research Study Assistant JobsClinical Research Study Assistant Jobs in Michigan

Clinical Research Study Assistant information

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$19

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How much do clinical research study assistant jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for clinical research study assistant in Michigan is $19.80, according to ZipRecruiter salary data. Most workers in this role earn between $15.10 and $22.64 per hour, depending on experience, location, and employer.

What skills and qualifications are needed to be a clinical research study assistant?

To thrive as a Clinical Research Study Assistant, you need a solid understanding of clinical research protocols, data collection, and regulatory compliance, often supported by a bachelor’s degree in a life science or related field. Familiarity with electronic data capture systems (EDC), Microsoft Office Suite, and Good Clinical Practice (GCP) certification is highly beneficial. Strong organizational skills, attention to detail, and effective communication set standout candidates apart. These skills are crucial for maintaining study integrity, ensuring accurate data, and supporting smooth collaboration across research teams.

What is the difference between Clinical Research Study Assistant vs Clinical Research Coordinator?

AspectClinical Research Study AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree or relevant certificationRequires a bachelor's degree, often with additional certifications or experience
Work EnvironmentAssists in data collection, documentation, and administrative tasks in clinical settingsManages study protocols, patient recruitment, and regulatory compliance in clinical trials
Employer & Industry UsageUsed by research institutions, hospitals, and pharmaceutical companiesCommonly employed in similar settings, often overseeing study operations

The Clinical Research Study Assistant primarily supports data collection and administrative tasks, while the Clinical Research Coordinator manages study protocols and patient interactions. Both roles are essential in clinical trials, with the coordinator typically having more responsibilities and requiring additional experience or certifications.

How does a clinical research study assistant collaborate with other members of the research team?

A Clinical Research Study Assistant works closely with principal investigators, study coordinators, and other research staff to ensure the smooth operation of clinical trials. Collaboration often involves coordinating participant scheduling, communicating protocol updates, and assisting with data collection and entry. These professionals also help ensure regulatory compliance by working with regulatory specialists and contribute to team meetings where study progress and challenges are discussed. Strong teamwork and communication skills are essential for successfully supporting the study's goals and maintaining high-quality research standards.

What does a clinical research study assistant do?

A Clinical Research Study Assistant supports the daily operations of clinical trials and research studies. Their tasks typically include preparing study materials, collecting and entering data, scheduling and coordinating participant visits, and ensuring that study protocols are followed. They may also assist with regulatory documentation and serve as a point of contact for study participants. This role is essential in helping research teams maintain accurate records and comply with ethical and legal standards. Clinical Research Study Assistants often work under the supervision of study coordinators or principal investigators.

What are the most commonly searched types of Clinical Research Study jobs in Michigan?

The most popular types of Clinical Research Study jobs in Michigan are:

What cities in Michigan are hiring for Clinical Research Study Assistant jobs?

Cities in Michigan with the most Clinical Research Study Assistant job openings:

Clinical Research Study Assistant jobs near you
Infographic showing various Clinical Research Study Assistant job openings in Michigan as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $41,175 per year, or $19.8 per hour.

Coordinator Clinical Research

McLaren

Flint, MI • On-site

$23.50 - $31.25/hr

Full-time

Re-posted 25 days ago

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
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About McLaren

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McLaren Group is globally renowned as one of the world’s most illustrious high-technology brands. Since the formation of McLaren Racing in 1963, McLaren has been pioneering and innovating in the competitive world of Formula 1, forging a formidable reputation which has seen the racing team win 20 World Championships and over 180 races. The Group has built on its successful racing expertise and diversified to include a global, high-performance sports car business, McLaren Automotive, and a game-changing technology and innovation business, McLaren Applied. Despite the broadening of the group’s business interests, McLaren’s goal remains singular: we exist to win in everything we do.

Industry

Automobile dealers and manufacturing

Company size

10,000+ Employees

Headquarters location

Woking, Surrey, GB

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