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Part Time Clinical Research Associate Jobs in Detroit, MI

Oral Surgeon

Shelby, MI · On-site

$267K - $353K/yr

Associate Oral Surgeon Opportunity Shelby Township, MI Shelby Oral Surgery Dr. Joseph M. Hildebrand ... Khazaal Part-Time Clinical Scope The ideal candidate will be comfortable providing a full range of ...

Oral Surgeon

Utica, MI

$276K - $364K/yr

Associate Oral Surgeon Opportunity - Shelby Township, MI Shelby Oral Surgery - Dr. Joseph M ... Khazaal - Part-Time Clinical Scope The ideal candidate will be comfortable providing a full range ...

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Part Time Clinical Research Associate information

See Detroit, MI salary details

$11

$40

$69

How much do part time clinical research associate jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for part time clinical research associate in Detroit, MI is $40.71, according to ZipRecruiter salary data. Most workers in this role earn between $28.56 and $52.12 per hour, depending on experience, location, and employer.

What is a part time clinical research associate?

Part-time Clinical Research Associates (CRAs) are professionals who monitor and manage clinical trials on a flexible or reduced-hour schedule, rather than full-time. They are responsible for ensuring that studies comply with regulatory requirements, collecting data, and acting as a liaison between clinical trial sites and sponsors. Part-time CRAs may work remotely or travel to research sites as needed, and their schedules can vary depending on the needs of the research project. This role is ideal for those seeking work-life balance or supplementing other professional activities. Their work is critical in advancing medical research and ensuring patient safety.

What are the key skills and qualifications needed to thrive as a part time clinical research associate?

To thrive as a Part Time Clinical Research Associate, you need a background in life sciences or healthcare, knowledge of clinical research protocols, and often a bachelor’s degree in a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certification such as ACRP or SOCRA is highly valued. Strong attention to detail, organizational skills, and effective communication are essential soft skills for monitoring trials and collaborating with research teams. These skills ensure regulatory compliance, accurate data collection, and efficient trial execution, all critical for successful clinical research outcomes.

What are some common challenges faced by part time clinical research associates, and how can they be managed effectively?

Part-time Clinical Research Associates (CRAs) often face the challenge of balancing multiple study sites and projects within limited working hours. Time management and clear communication with both the research team and site staff are crucial to ensure all monitoring visits, documentation, and regulatory requirements are met on schedule. Additionally, part-time CRAs may need to be proactive in staying updated on study protocols and industry regulations, as they may not be present for all in-person team meetings. Establishing structured routines and leveraging digital tools for remote collaboration can help manage these challenges effectively.

What is the difference between Part Time Clinical Research Associate vs Clinical Research Coordinator?

AspectPart Time Clinical Research AssociateClinical Research Coordinator
CredentialsBachelor's degree, often certifications like CCRP or RACBachelor's degree, often certifications like CCRP or RAC
Work EnvironmentMonitoring clinical trials at sites, remote or onsiteManaging trial operations at research sites
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinics
Search & Comparison IntentUnderstanding monitoring roles in trialsManaging trial activities at sites

Part Time Clinical Research Associates primarily focus on monitoring clinical trial progress, ensuring compliance, and verifying data accuracy, often working remotely or onsite. Clinical Research Coordinators handle the day-to-day operations at research sites, including patient recruitment and data collection. Both roles require similar credentials but differ in responsibilities and work settings.

What are the most commonly searched types of Part Time Clinical Research jobs in Detroit, MI?

The most popular types of Part Time Clinical Research jobs in Detroit, MI are:

What are popular job titles related to Part Time Clinical Research Associate jobs in Detroit, MI?

For Part Time Clinical Research Associate jobs in Detroit, MI, the most frequently searched job titles are:

What job categories do people searching Part Time Clinical Research Associate jobs in Detroit, MI look for?

The top searched job categories for Part Time Clinical Research Associate jobs in Detroit, MI are:

Infographic showing various Part Time Clinical Research Associate job openings in Detroit, MI as of August 2026, with employment types broken down into 100% Part Time. Highlights an 100% In-person job distribution, with an average salary of $84,683 per year, or $40.7 per hour.

Research Technician Intermediate

University of Michigan

Ann Arbor, MI • On-site

$17.50 - $24.25/hr

Part-time

Re-posted 24 days ago


University Of Michigan rating

8.0

Company rating: 8.0 out of 10

Based on 147 frontline employees who took The Breakroom Quiz

191st of 631 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.
Job Summary
The Michigan Clinical Trial Support Unit Clinical Research Coordinator Unit (M-CTSU CRC Unit) is seeking a part-time Clinical Research Intern to support clinical research activities while gaining structured, hands-on experience in research coordination.
This paid, term-limited position is designed for an individual interested in developing a deeper understanding of clinical research processes, including regulatory compliance, research documentation, participant-facing activities, data management, and research ethics. The selected candidate will work under the guidance of experienced clinical research professionals and receive training, mentorship, and regular feedback throughout the appointment.
The position will provide moderately complex technical and administrative support for clinical research projects. The anticipated appointment is approximately 20 hours per week from September 2026 through May 2027.
Responsibilities*
The University of Michigan offers a collaborative environment in which employees can contribute to research that advances health and improves patient care. In this position, you will have opportunities to:
  • Gain practical experience with clinical research operations
  • Learn about institutional, federal, and study-specific research requirements
  • Work alongside experienced clinical research coordinators and other research professionals
  • Participate in structured training, professional-development activities, and regular mentorship
  • Build skills in research documentation, data management, communication, organization, and ethical decision-making
  • Learn about career paths in clinical research, medicine, and related health professions

The M-CTSU Clinical Research Intern will work under the direct guidance of experienced clinical research staff and will assist team members who hold delegated study responsibilities. The intern will not independently manage studies, perform project-specific responsibilities, or make decisions regarding participant eligibility, informed consent, protocol implementation, or regulatory compliance.
Responsibilities may include:
  • Attend and actively contribute to the unit?s weekly education and training events, including discussions, presentations, workshops, and other professional-development activities.
  • Assist delegated study-team members with research documentation, regulatory materials, data collection and entry, data-quality review, and maintenance of study files.
  • Observe and support approved participant recruitment, scheduling, study visits, and follow-up activities under appropriate supervision.
  • Conduct literature searches and help organize or summarize information relevant to ongoing research projects.
  • Assist with reports, presentations, educational materials, and other research-related projects.
  • Participate in study-team and unit meetings and communicate progress, questions, and observations to the appropriate team members.
  • Complete required institutional, privacy, safety, and research training, including applicable CITI and PEERRS modules.
  • Maintain participant confidentiality, data integrity, and compliance with study protocols, institutional policies, and applicable regulations.
  • Meet regularly with an assigned supervisor or mentor to receive guidance, discuss learning goals, and review progress
  • Perform other related duties as assigned.

All activities will be performed within the intern?s documented training and authorization and under the oversight of qualified research personnel. Duties may vary based on unit needs, available learning opportunities, and the intern?s demonstrated competencies.
Supervision Received:
This position receives direct supervision and reports directly to the MCTSU Unit Administrator.
Supervision Exercised:
None
Required Qualifications*
High school diploma or GED is necessary.
Desired Qualifications*
Bachelor?s Degree in Health Science or an equivalent combination of related education and experience is desirable. An understanding of medical terminology, experience in a large complex health care setting, ability to effectively communicate with staff and faculty of all levels, and knowledge of university policies and procedures is desirable.
Modes of Work
The work requires, or the supervisor approves a fully onsite presence. Onsite is defined as a designated U-M owned or leased work location within or outside of the State of Michigan.
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 .
Work Schedule
This is a 50% FTE position requiring approximately 20 hours per week. The schedule will be established in consultation with the selected candidate and the unit based on operational and study needs.
Work will occur during standard weekday business hours to support research-participant visits, training sessions, and study-team meetings. The position is expected to be primarily on-site at University Hospital South in Ann Arbor. Eligibility for remote work, if any, will depend on assigned responsibilities, data-access requirements, and unit policy.
Background Screening
The University of Michigan conducts background checks on all job candidates upon acceptance of a contingent offer and may use a third party administrator to conduct background checks. Background checks are performed in compliance with the Fair Credit Reporting Act.
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
282651
Working Title
Research Technician Intermediate
Job Title
Research Tech Intermediate
Work Location
Ann Arbor Campus
Ann Arbor, MI
Modes of Work
Hybrid
Full/Part Time
Part-Time
Regular/Temporary
Regular
FLSA Status
Nonexempt
Organizational Group
Medical School
Department
MM Research-Clin Trial Units
Posting Begin/End Date
9/03/2026 - 9/10/2026
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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