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Clinical Study Assistant Jobs in Michigan (NOW HIRING)

Assemble study kits for study visits * Attend and participate in study meetings, SIVs, monitoring visits and other sponsor and regulatory meetings * Complete Data Entry for studies both in sponsor ...

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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... assist with the build of the clinical study systems used at trial sites. Key Responsibilities Clinical system support: * Own system-level builds and testing for the clinical study device platform ...

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Clinical Study Assistant information

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$10

$17

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How much do clinical study assistant jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for clinical study assistant in Michigan is $17.63, according to ZipRecruiter salary data. Most workers in this role earn between $14.47 and $20.34 per hour, depending on experience, location, and employer.

What are the main challenges a clinical study assistant might face when supporting clinical trial operations?

A Clinical Study Assistant often encounters challenges such as managing multiple tasks under tight deadlines, ensuring accurate documentation, and coordinating communication between research teams, sponsors, and regulatory bodies. Additionally, adapting to evolving study protocols and maintaining compliance with strict regulatory requirements can be demanding. Strong organizational skills, attention to detail, and proactive communication are essential for navigating these challenges successfully.

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

AspectClinical Study AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related fieldUsually requires a bachelor's degree, often with additional certifications in clinical research
Work EnvironmentSupports clinical trials in hospitals, research centers, or pharmaceutical companiesManages entire clinical studies, coordinating between sites, staff, and sponsors
Employer & IndustryHospitals, research institutions, pharmaceutical companiesAcademic medical centers, hospitals, research organizations
Search & Comparison IntentOften compared for entry-level roles supporting clinical trialsCompared for roles with broader responsibilities in clinical study management

The Clinical Study Assistant primarily supports clinical trial activities by assisting with data collection and documentation, while the Clinical Research Coordinator manages the overall conduct of the study, including patient recruitment and compliance. Both roles require similar educational backgrounds but differ in scope and responsibilities within the clinical research process.

What is a clinical study assistant?

Clinical Study Assistants are professionals who support the conduct of clinical trials by handling administrative tasks, maintaining study documentation, and ensuring regulatory compliance. They work closely with clinical research teams to coordinate schedules, communicate with study sites, and help manage trial materials. Their role is crucial in ensuring that clinical studies run smoothly, efficiently, and according to protocols and regulatory guidelines.

What are the key skills and qualifications needed to thrive as a clinical study assistant?

To thrive as a Clinical Study Assistant, you need strong organizational skills, attention to detail, and a background in life sciences or related fields, often supported by a bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and regulatory documentation processes is typically required. Effective communication, teamwork, and problem-solving skills help you navigate complex study protocols and collaborate with diverse stakeholders. These abilities are crucial for ensuring the accuracy, compliance, and smooth operation of clinical research studies.
What are the most commonly searched types of Clinical Study jobs in Michigan? The most popular types of Clinical Study jobs in Michigan are:
Infographic showing various Clinical Study Assistant job openings in Michigan as of August 2026, with employment types broken down into 2% As Needed, 72% Full Time, 19% Part Time, and 7% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $36,676 per year, or $17.6 per hour.

Clinical Study Coordinator

University of Michigan

Ann Arbor, MI • On-site

$50K - $60K/yr

Full-time

Medical, Life, Retirement

Posted 4 days ago


University Of Michigan rating

8.1

Company rating: 8.1 out of 10

Based on 144 frontline employees who took The Breakroom Quiz

158th of 617 rated colleges and universities


Job description

How to Apply
To apply for this job, please upload (combined into ONE PDF) a CV/resume, cover letter, and the names/contact information for 3 professional references. The cover letter should address your specific interest in the position and outline the skills and experience that directly relate to this position. All inquiries about the position should be emailed to Dr. David Lipps ( [email protected] ) with the subject line "LETS MOVE Clinical Study Coordinator Inquiry".
Job Summary
The School of Kinesiology , in partnership with the Rogel Cancer Center, is launching LETS MOVE, a structured exercise program for patients with cancer. The School of Kinesiology (PIs: David Lipps, Erin Giles, Angela Fong, Elizabeth Salerno) is seeking a full-time Clinical Study Coordinator (CSC) to join the team.
In this role, the CSC will provide administrative oversight and study coordination of the LETS MOVE trial. The CSC responsibilities may involve interfacing with study participants and administrative and regulatory oversight of research projects, including, but not limited to, monitoring study progress, ensuring research protocol and regulatory compliance, and producing study reports. The successful candidate will be reliable, conscientious, organized, and able to work independently with minimal supervision.
Responsibilities*
Essential Functions are noted with an "EF"
Research coordination and administration tasks (50%)
  • Identify research participants (e.g., Emerse, DataDirect, and MiChart/Epic), determine eligibility, and consent eligible participants
  • Schedule and monitor the delivery of assessments within a patient-facing application (MyDataHelps) (EF)
  • Develop and maintain project databases and participant tracking spreadsheets using REDCap, Excel, OnCore, and Velos. (EF)
  • Regulatory management of research (e.g., IRB applications, eResearch), monitor study progress, and producing regular study reports including NIH progress reports. (EF)
  • Administer data-collection instruments online, in person, or by phone.

General administration tasks (50%)
  • Coordinates interactions with collaborating cancer care teams in the Rogel Cancer Center, including physicians, advanced practice providers, and support staff. (EF)
  • Managing the training of study personnel. (EF)
  • Grant, abstract, and manuscript preparation support such as conducting literature reviews, managing references, and manuscript submission coordination.
  • Assist with data analysis and management as needed.
  • Performs other related duties as assigned.

Required Qualifications*
  • A bachelor's degree in health science or a related field (e.g., kinesiology, public health, epidemiology, exercise or health science, health education and health promotion, medicine, psychology) or an equivalent combination of related education and experience.
  • A minimum of 2 years of related research coordination or equivalent experience is required.
  • Must be able to demonstrate proven organizational, coordination and problem-solving skills, with high attention to detail.
  • Demonstrated ability to work independently and take initiative, yet seek supervision, as appropriate.
  • Formal training or experience in database creation and management or research methods and statistics.
  • Ability to remain stationary at a computer for up to 4 hours to collect, process, or review data.
  • Proven ability to contribute to a positive workplace culture and demonstrate the school's core values.

Desired Qualifications*
  • A master's degree in health science or related field with at least 1 year of related research experience.
  • Prior experience with cancer research preferred or prior research coordination responsibilities in academic medical settings.
  • Prior experience working with electronic hospital records (MiChart/Epic) or research coordinator platforms (OnCore, Velos)
  • Familiarity with or ability to quickly learn University of Michigan research-related organizational structure, policies, and procedures.

Why Work at Michigan?
In addition to a career filled with purpose and opportunity, The University of Michigan offers a comprehensive benefits package to help you stay well, protect yourself and your family and plan for a secure future. Benefits include:
  • Generous time off
  • A retirement plan that provides two-for-one matching contributions with immediate vesting
  • Many choices for comprehensive health insurance
  • Life insurance
  • Long-term disability coverage
  • Flexible spending accounts for healthcare and dependent care expenses
  • Maternity and parental leave
  • University commitment to providing reasonable accommodations to individuals with disabilities

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 .
Additional Information
The position is available immediately and is term-limited, funded for 18 months; the initial appointment may be extended depending on performance and availability of research funds. The salary range is $50,000 to $60,000, commensurate with education and experience. You are encouraged to discuss salary questions to honor understanding and transparency throughout the recruiting process.
This is an onsite position, located at the School of Kinesiology offices at Domino's Farms (24 Frank Lloyd Wright Drive Ann Arbor, Mi 48106), with the potential to transition to hybrid work after initial familiarization with lab procedures, space, and equipment. Candidates interested in hybrid work should indicate this to the hiring manager during the recruiting process.
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 will be 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 any time 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
281196
Working Title
Clinical Study Coordinator
Job Title
Clinical Research Coord Assoc
Work Location
Ann Arbor Campus
Ann Arbor, MI
Modes of Work
Onsite
Full/Part Time
Full-Time
Regular/Temporary
Regular
FLSA Status
Nonexempt
Organizational Group
School Kinesiology
Department
School of Kinesiology
Posting Begin/End Date
8/05/2026 - 8/19/2026
Salary
$50,000.00 - $60,000.00
Career Interest
Research

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About University of Michigan

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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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