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Clinical Research Associate Intern Jobs in Michigan

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Clinical Research Associate Intern information

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$1.8K

$5.6K

$6.8K

How much do clinical research associate intern jobs pay per month?

As of Aug 23, 2026, the average monthly pay for clinical research associate intern in Michigan is $5,612.67, according to ZipRecruiter salary data. Most workers in this role earn between $3,850.00 and $6,683.33 per month, depending on experience, location, and employer.

What does a clinical research associate intern do?

A Clinical Research Associate Intern assists in the monitoring and coordination of clinical trials to ensure they are conducted according to regulatory standards and study protocols. Interns may help with site visits, data collection, documentation, and communication between research teams and sponsors. This role provides hands-on experience in clinical research processes and helps interns develop an understanding of Good Clinical Practice (GCP) guidelines. Interns often work under the supervision of experienced clinical research professionals and gain valuable insight into the pharmaceutical or medical device industry.

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

To thrive as a Clinical Research Associate Intern, you need a solid understanding of clinical trial protocols, regulatory guidelines (like GCP), and typically a background in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and sometimes certifications like GCP training are highly valued. Strong attention to detail, organizational skills, and effective communication help interns excel in monitoring studies and collaborating with site staff. These skills are crucial for ensuring data integrity, regulatory compliance, and the smooth operation of clinical research projects.

What typical challenges do clinical research associate interns encounter when monitoring clinical trial sites?

Clinical Research Associate Interns often face challenges such as ensuring accurate data collection, maintaining regulatory compliance, and communicating effectively with site staff. Balancing these responsibilities while learning industry protocols can be demanding, especially when managing multiple sites or studies. Interns are supported by experienced team members, but must quickly adapt to varying site workflows and documentation standards to ensure trial integrity.

What is the difference between Clinical Research Associate Intern vs Clinical Research Coordinator?

AspectClinical Research Associate InternClinical Research Coordinator
Required CredentialsTypically pursuing or holding a degree in life sciences; some internships require minimal certificationsUsually holds a bachelor's degree in health sciences or related field; certifications like CCRP are common
Work EnvironmentInternship setting within pharmaceutical companies or research institutions; supervised learningActive role in clinical trial sites; responsible for daily trial operations
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and research institutions for trainingEmployed directly at clinical sites, hospitals, or research centers

While both roles involve clinical trial processes, a Clinical Research Associate Intern is primarily a learning position focusing on gaining experience, whereas a Clinical Research Coordinator manages the day-to-day operations of clinical trials at research sites.

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

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

What are popular job titles related to Clinical Research Associate Intern jobs in Michigan?

For Clinical Research Associate Intern jobs in Michigan, the most frequently searched job titles are:

What cities in Michigan are hiring for Clinical Research Associate Intern jobs?

Cities in Michigan with the most Clinical Research Associate Intern job openings:

Infographic showing various Clinical Research Associate Intern job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 66% Full Time, 27% Part Time, 3% Temporary, 2% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $67,352 per year, or $32.4 per hour.

Clinical Research Technician (Underfill)

University of Michigan

Ann Arbor, MI • On-site

Full-time

Medical, Dental, Vision, Retirement

Posted 15 days ago


University Of Michigan rating

8.1

Company rating: 8.1 out of 10

Based on 145 frontline employees who took The Breakroom Quiz

168th of 622 rated colleges and universities


Job description

How to Apply
A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position.
Mission Statement
Michigan Medicine improves the health of patients, populations and communities through excellence in education, patient care, community service, research and technology development, and through leadership activities in Michigan, nationally and internationally. Our mission is guided by our Strategic Principles and has three critical components; patient care, education and research that together enhance our contribution to society.
Job Summary
As an integral member of the research team, the Clinical Research Technician (CRT) will help ensure that clinical research studies supported by the University of Michigan Kellogg Clinical Research Center (KCRC) are initiated and executed in the highest quality and compliant manner. In order to succeed, the applicant must possess exceptional organizational skills, uncompromising integrity, a love of people, and a strong willingness to learn new skills. .
Responsibilities*
COMMUNICATIONS: The CRT is expected to facilitate communications between research volunteers,
study team members, and investigators. The communications will include, but are not limited to scheduling appointments, meeting with study team members and investigators, and resolving issues that invariably arise.
PATIENT INTERACTION: At study visits, the CRT will collect past medical history, concomittant medications, and adverse events, and then take research patients through the protocol schedule of activities for each visit. The CRT will perform majority of the required testing (visual acuity, contrast sensitivity, visual fields, vital signs, EKGs, blood draws, etc.) and scribe for our physicians while they perform eye exams on patients. The CRT may help with recruitment efforts and obtaining patient consent.
DATA: The CRT will input the data collected into case report forms and/or electronic data capture systems, maintain studies in the OnCore clinical trial management system, and resolve queries.
REGULATORY COMPLIANCE: The CRT is expected to ensure that all research is conducted safely and according to protocol. This includes an understanding of good clinical practice (GCP) and ensuring compliance with federal, state, and sponsor policies.
PROTOCOL SPECIFIC NEEDS: In addition to the broad technical skills needed in nearly every ophthalmic clinical study (e.g. visual acuity, refraction, intraocular pressure, etc.), each study often has unique needs. The CRT is expected to possess a willingness to learn protocol specific requirements. Some of our clinical trials may require ordering and handling investigational product.
OTHER: Clinical research regulations and best practices are frequently changing. The CRT is expected to incorporate these changes into the work flow as they occur. In addition, the CRT will need to become proficient with phlebotomy and acquire various certifications pertinent to the position.
Required Qualifications*
For a Clinical Research Technician level position:
  • Associate degree in Health Science or an equivalent combination of related education and experience.Associate degree in Health Science or an equivalent combination of related education and experience.
  • ONE of the following:
  • Minimum 1 years of direcUy related experience in clinical research and clinical trials is necessary. Please review SoCRA's Definition of a Clinical Research Professional qualifying experience prior to applying.
  • An advanced degree in a health-related areas such as: Health Sciences, Behavioral Sciences, Public Health, Health Care Administration, Clinical Research Administration, Social Work, Psychology, Epidemiology, Foreign MD.
  • Minimum 3 years of human subject experience (clinical, lab or health regulations) such as related patient care, related community health and wellness, related clinical information, and research.

For a Clinical Research Assistant level position:
High school diploma or GED is necessary, with an Associate Degree in Health Science or an equivalent combination of related education and experience preferred.
Directly related experience in clinical research and clinical trials is preferred but not necessary.
All levels will reguire:
Professional demeanor and excellent interpersonal and communication skills.
Experience with Microsoft Office products (i.e., Microsoft Word, Excel, and Power Point)
Confident and highly motivated with excellent multi-tasking ability and record-keeping skills.
Outstanding organizational skills with meticulous attention to detail.
Strong ability to work independently, exercising good judgement, with minimal supervision.
Ability to function with diverse teams of people in a diplomatic, collaborative, and effective manner.
Strong problem-solving skills.
Demonstrated ability to learn and use new skills quickly and effectively.
Able to maintain data confidentiality and participanVsubjecVpatient privacy.
Excellent attendance record and strong work ethic.
Desired Qualifications*
- Bachelor's degree in Health Science or an equivalent combination of related education and experience.
- An understanding of medical terminology.
- Ability to effectively communicate with staff and faculty of all levels.
- At least one year of directly related experience in clinical research and clinical trials.
- Experience as an ophthalmic assistant or equivalent.
- Previous experience with EMR/Epic, MiChart, eReseach, OnCore
Why Join Michigan Medicine?
Michigan Medicine is one of the largest health care complexes in the world and has been the site of many groundbreaking medical and technological advancements since the opening of the U-M Medical School in 1850. Michigan Medicine is comprised of over 30,000 employees and our vision is to attract, inspire, and develop outstanding people in medicine, sciences, and healthcare to become one of the world's most distinguished academic health systems. In some way, great or small, every person here helps to advance this world-class institution. Work at Michigan Medicine and become a victor for the greater good.
What Benefits can you Look Forward to?
  • Excellent medical, dental and vision coverage effective on your very first day
  • 2:1 Match on retirement savings

Modes of Work
Positions that are eligible for hybrid or mobile/remote work mode are at the discretion of the hiring department. Work agreements are reviewed annually at a minimum and are subject to change at any time, and for any reason, throughout the course of employment. Learn more about the work modes .
Underfill Statement
This position may be underfilled at a lower classification depending on the qualifications of the selected candidate.
Background Screening
Michigan Medicine conducts background screening and pre-employment drug testing on job candidates upon acceptance of a contingent job offer and may use a third party administrator to conduct background screenings. Background screenings are performed in compliance with the Fair Credit Report Act. Pre-employment drug testing applies to all selected candidates, including new or additional faculty and staff appointments, as well as transfers from other U-M campuses.
Application Deadline
Job openings are posted for a minimum of seven calendar days. The review and selection process may begin as early as the eighth day after posting. This opening may be removed from posting boards and filled anytime after the minimum posting period has ended.
U-M EEO Statement
The University of Michigan is an Equal Opportunity Employer. We are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants, including protected veterans and individuals with disabilities.
Job Detail
Job Opening ID
281731
Working Title
Clinical Research Technician (Underfill)
Job Title
Clinical Research Technician
Work Location
Ann Arbor Campus
Ann Arbor, MI
Modes of Work
Hybrid
Full/Part Time
Full-Time
Regular/Temporary
Regular
FLSA Status
Nonexempt
Organizational Group
Medical School
Department
MM Ophthal. & Visual Science
Posting Begin/End Date
8/17/2026 - 8/31/2026
Career Interest
Research

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About University of Michigan

Sourced by ZipRecruiter

The University of Michigan (U-M), based in Ann Arbor, MI, US, is one of America's most esteemed institutions in higher education. Established in 1817, it presides in the industry of education and research, providing a range of services including undergraduate, graduate, and professional education programs. Complementing this is an extensive research activity that has significantly contributed to various fields, from healthcare to engineering, humanities to sports. Upholding its mission "to serve the people of Michigan and the world through preeminence in creating, communicating, preserving and applying knowledge, art, and academic values", U-M consistently ranks among the top universities globally, a testament to its tradition of excellence in learning and research, and a deep commitment to innovation and discovery.

Industry

Colleges, universities, and professional schools

Company size

10,000+ Employees

Headquarters location

Ann Arbor, MI, US

Year founded

1817

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