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Study Coordinator Jobs (NOW HIRING)

This position involves coordination of multiple ongoing research studies in children and adults using MRI, EEG, brain stimulation, and behavioral data collection to investigate the neurophysiological ...

New

Study Coordinator Madison WI Labcorp is seeking a Study Coordinator to join our Toxicology team in Madison, WI. Job Responsibilities: The Study Coordinator is responsible for providing highlevel ...

Manager, Study Coordination & Quality Control Join a team driven by science, powered by people, and committed to improving lives. A GLP public CRO is seeking an experienced and passionate Manager ...

Assists in the coordination of study tasks from pre-study initiation to study completion. Performs accurate and timely record keeping consistent with the maintenance of facility SOPs. Utilizes ...

The Study Coordinator provides critical operational and project management support to the Study Director in GLP-regulated preclinical studies for Neuralink devices. This role handles the majority of ...

Study Coordinator

Boulder, CO · On-site

$27 - $34/hr

The Study Coordinator reports to the Study Coordinator Supervisor within the In Vivo Department with responsibilities centered around supporting all functions of the preclinical study process. The ...

The Study Coordinator reports to the Study Coordinator Supervisor within the In Vivo Department with responsibilities centered around supporting all functions of the preclinical study process. The ...

Study Coordinator

Denver, CO · On-site

$60K - $75K/yr

Overview Rocky Mountain Cancer Centers, Colorado's largest and most comprehensive provider of cancer care has an exciting opportunity for an experienced Research Study Coordinator in Denver Bring ...

As the Study Coordinator you will plan the execution and monitor the completion of complex Phase I-IV assigned clinical research protocols. Including abstracting, assembling and organizing research ...

The Study Coordinator II provides advanced coordination and operational support for governmentled clinical and translational research studies. Working under the direction of the Principal ...

Study Coordinator

Denver, CO · On-site

$60K - $75K/yr

Overview Rocky Mountain Cancer Centers, Colorado's largest and most comprehensive provider of cancer care has an exciting opportunity for an experienced Research Study Coordinator in Denver Bring ...

The Study Coordinator provides critical operational and project management support to the Study Director in GLP-regulated preclinical studies for Neuralink devices. This role handles the majority of ...

Study Coordinator

Washington, DC · On-site

$50K - $60K/yr

To coordinate study participants in the Clinical Trials Unit. Execute tasks as required by the study protocols. SUPERVISORY AUTHORITY: Involves no responsibility or authority for the direction of ...

Summary The purpose of the Study Coordinator I position is to support the execution of in vitro and in vivo pharmacology studies by coordinating the technical execution of projects. This Study ...

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Study Coordinator information

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$22K

$54.9K

$80.5K

How much do study coordinator jobs pay per year?

As of Jul 19, 2026, the average yearly pay for study coordinator in the United States is $54,853.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $62,500.00 per year, depending on experience, location, and employer.

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

To thrive as a Study Coordinator, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, usually backed by a bachelor’s degree in a science or health-related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification is typically required. Strong organizational skills, attention to detail, and effective communication help you manage study logistics and collaborate with research teams and participants. These skills ensure that studies are conducted ethically, efficiently, and in accordance with regulatory standards.

What Is a Study Coordinator?

A study coordinator works in a clinical research environment. In this position, your job duties are to oversee the day-to-day operations of a given study under the guidance of a research director. You direct tests, ensure all research is done according to ethical standards, and ensure the comfort and safety of subjects. As a study coordinator, you also ensure all patients provide informed consent prior to participation. Overall, your responsibility is to provide a safe environment for the study. To be a study coordinator, the qualifications are usually a bachelor’s degree or an RN degree. You typically need several years of experience in a clinical setting, and you must demonstrate skills in research.

How much does a CRC make?

In Ohio, a Clinical Research Coordinator (CRC) typically earns between $45,000 and $65,000 annually, depending on experience, certifications, and the employer. Entry-level CRCs may start at lower salaries, while those with specialized skills or certifications can earn higher wages. The role often requires knowledge of regulatory compliance and data management tools.

What is a study coordinator?

A study coordinator is a professional responsible for managing and overseeing clinical research studies or trials. They coordinate activities such as participant recruitment, data collection, and compliance with protocols, often working closely with researchers and healthcare providers. Strong organizational skills and knowledge of regulatory requirements are essential for this role.

What are study coordinators?

Study coordinators are professionals who manage the day-to-day operations of clinical research studies. They are responsible for tasks such as recruiting participants, ensuring protocol compliance, collecting and managing data, and maintaining communication between investigators, participants, and regulatory bodies. Study coordinators play a vital role in making sure that research studies are conducted ethically, efficiently, and according to regulatory guidelines. Their work ensures the integrity of study data and the safety of participants throughout the research process.

What are some common challenges Study Coordinators face when managing multiple clinical trials simultaneously?

Study Coordinators often juggle several clinical trials at once, each with its own protocols, timelines, and regulatory requirements. Keeping track of participant enrollment, data collection, and compliance across different studies can be demanding and requires strong organizational skills. Effective communication with investigators, sponsors, and other team members is crucial to prevent errors, ensure deadlines are met, and maintain the quality of study data. Using robust tracking systems and prioritizing tasks can help manage these challenges efficiently.

What is the difference between Study Coordinator vs Research Assistant?

AspectStudy CoordinatorResearch Assistant
Required CredentialsTypically a bachelor's degree in health sciences, biology, or related fieldOften a bachelor's degree or current student in a related field
Work EnvironmentClinical research settings, hospitals, or research institutionsLaboratories, research centers, or clinical sites
Employer & Industry UsageUsed by hospitals, universities, and research organizationsCommonly employed in academic and research institutions
Common Search & Comparison IntentUnderstanding roles, responsibilities, and qualificationsLearning about entry-level research roles and support tasks

The Study Coordinator and Research Assistant roles share similarities in working within research environments and requiring related educational backgrounds. However, Study Coordinators typically have more responsibilities in managing study protocols and participant coordination, while Research Assistants focus on supporting research activities and data collection. Both roles are essential in advancing clinical research and often work closely together in research projects.

How much does a study coordinator earn?

A study coordinator's average salary varies by experience and location but typically ranges from $45,000 to $70,000 annually. Entry-level coordinators may earn around $40,000, while those with more experience or specialized skills can earn over $80,000. The role often requires knowledge of clinical research protocols and data management tools.

Is CRC an entry level position?

A Clinical Research Coordinator (CRC) is often considered an entry-level position in clinical research, suitable for individuals with a bachelor's degree in a related field. However, some employers may prefer candidates with prior experience or certifications such as the Certified Clinical Research Coordinator (CCRC).
What cities are hiring for Study Coordinator jobs? Cities with the most Study Coordinator job openings:
What are the most commonly searched types of Study jobs? The most popular types of Study jobs are:
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What states have the most Study Coordinator jobs? States with the most job openings for Study Coordinator jobs include:
Infographic showing various Study Coordinator job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $54,853 per year, or $26.4 per hour.
Study Coordinator

Full-time

Medical, Dental, Vision, Retirement

Posted 3 days ago

New


University Of Michigan rating

8.2

Company rating: 8.2 out of 10

Based on 142 frontline employees who took The Breakroom Quiz

122nd of 555 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
We are seeking applicants for a full-time Research Technician Intermediate to support the Speech Neurophysiology Lab (PI: Soo-Eun Chang). Applicants are encouraged to visit our website to learn more about ongoing projects. This position involves coordination of multiple ongoing research studies in children and adults using MRI, EEG, brain stimulation, and behavioral data collection to investigate the neurophysiological basis of developmental stuttering. Primary responsibilities are day-to-day coordination and execution of research studies, including participant recruitment, scheduling, community outreach, data collection, and study coordination.
Responsibilities*
The statements included in this description are intended to reflect the general nature and level of work assigned to this role and should not be interpreted as all-inclusive.
Responsibilities may include:
  • Participant recruitment, screening, enrollment, scheduling, and follow-up communications via telephone, email, videoconferencing platforms, and other approved methods.
  • Conducting study visits and research assessments with participants (data collection using behavioral, physiological, neuroimaging, and other research methods as required by individual projects)
  • Coordinating communication with participants, families, schools, community organizations, and other stakeholders.
  • Supporting community outreach, recruitment events, educational activities, and participant engagement efforts.
  • Assisting with study coordination and tracking participant progress through research protocols.
  • Maintaining detailed study records, research databases, and regulatory documentation.
  • Performing data entry, data verification, and quality assurance procedures.
  • Preparing, organizing, and ordering study materials and supplies as needed.
  • Monitoring study progress and supporting multiple projects simultaneously.
  • Attending weekly team meetings and required trainings.
  • Other duties as assigned to support laboratory operations and research activities.

Required Qualifications*
  • HS Diploma or Associate Degree in communication sciences and disorders, psychology, neuroscience, linguistics, education, public health, or a related field.
  • 1 year of direct experience collecting data from research participants in a research or clinical setting.
  • Comfort and experience interacting directly with children (and their parents) and adults as participants.
  • Comfort attending community outreach activities (e.g., tabling at local health fairs, conferences, etc.).
  • Comfort making phone calls, handling unexpected issues, and adapting to changing study needs.
  • Ability to receive and incorporate frequent corrective feedback, particularly during training.
  • Ability to work independently and as part of a collaborative research team.
  • Strong interpersonal skills and comfort interacting with research participants of diverse backgrounds and ages.
  • Excellent attention to detail and the ability to precisely follow multi-step protocols.
  • Ability to assume responsibility, meet data deadlines, and maintain confidentiality.
  • Excellent organizational, verbal, and written communication skills.
  • Proficiency in computer skills, including Microsoft software applications as well as electronic databases.
  • Ability to be punctual and work within tight deadlines.
  • Maintain professional and technical knowledge.

Desired Qualifications*
  • Bachelor's degree (or equivalent education and experience) in communication sciences and disorders, psychology, neuroscience, linguistics, education, public health, or a related field.
  • 2+ years of directly relevant experience: research, clinical, educational, or community-engagement experience (this can include experience obtained during undergraduate studies).
  • Previous employment (outside of undergraduate studies) as a research assistant, study coordinator, or in a participant-facing research environment.
  • Interest in speech, language, communication, cognitive, or neurodevelopmental research.
  • Familiarity with REDCap, Qualtrics, or other research management systems.
  • Experience coordinating multiple projects and competing priorities.

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 .
Work Schedule
This is a Monday through Friday, full-time, on-site position. This position requires some flexible scheduling of evening and weekend work around busy periods of data collection and community events. Our priority is to schedule research visits at the most convenient time for our participants, who may require after school or after work sessions
Work Locations
This position is located at one of our off-site campus locations in Ann Arbor, MI.
Additional Information
Successful candidates will be joining a collaborative research environment that supports professional development and skill building in research methods, participant engagement, and study coordination. A team science approach is central to our lab. Proactive collaboration, professionalism, and willingness to support team members are expected.
The primary focus of this position is the successful execution of ongoing research studies. Opportunities to contribute to data analysis, manuscript preparation, conference presentations, and independent research projects may become available after the candidate has demonstrated excellence in core research assistant responsibilities.
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.
In addition to the screenings indicated above under Michigan law, a criminal history check including fingerprinting is required as a condition of transfer or employment for this position.
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.
E-Verify
The University of Michigan participates with the federal EVerify system. Individuals hired into positions that are funded by a federal contract with the FAR EVerify clause must have their identity and work eligibility confirmed by the EVerify system. This position is identified as a position that may include the EVerify requirement.
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
279877
Working Title
Study Coordinator
Job Title
Research Tech Intermediate
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
Medical School
Department
MM Psychiatry Child Services
Posting Begin/End Date
7/16/2026 - 1/08/2027
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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