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Clinical Research Coordinator Jobs in Toledo, OH

Harbor is looking for a Clinical Coordinator who works in a highly collaborative manner with Physician Led Patient Centered team staff to ensure overall team success in patient centered service ...

Harbor is looking for a Clinical Coordinator who works in a highly collaborative manner with Physician Led Patient Centered team staff to ensure overall team success in patient centered service ...

As a Physician Services Clinical Coordinator, you'll ensure that elderly patients receive seamless, coordinated care by managing provider orders, coordinating services, and serving as a knowledgeable ...

As a Physician Services Clinical Coordinator, you'll ensure that elderly patients receive seamless, coordinated care by managing provider orders, coordinating services, and serving as a knowledgeable ...

As a Physician Services Clinical Coordinator, you'll ensure that elderly patients receive seamless, coordinated care by managing provider orders, coordinating services, and serving as a knowledgeable ...

As a Physician Services Clinical Coordinator, you'll ensure that elderly patients receive seamless, coordinated care by managing provider orders, coordinating services, and serving as a knowledgeable ...

Clinical Therapist II

Bowling Green, OH

$55.80K - $75.10K/yr

Provide crisis assessments, stabilization, and service coordination in order to de-escalate crisis ... Participates in agency-wide and departmental clinical research as needed. * Participates in program ...

Clinical Therapist II

Perrysburg, OH · On-site

$56.10K - $75.40K/yr

Provide crisis assessments, stabilization, and service coordination in order to de-escalate crisis ... Participates in agency-wide and departmental clinical research as needed. * Participates in program ...

Clinical Therapist II

Bowling Green, OH · On-site

$55.80K - $75.10K/yr

Provide crisis assessments, stabilization, and service coordination in order to de-escalate crisis ... Participates in agency-wide and departmental clinical research as needed. * Participates in program ...

Clinical Therapist II

Perrysburg, OH

$56.10K - $75.40K/yr

Provide crisis assessments, stabilization, and service coordination in order to de-escalate crisis ... Participates in agency-wide and departmental clinical research as needed. * Participates in program ...

Clinical Therapist I

Toledo, OH · On-site

$58.10K - $78.20K/yr

Provide crisis assessments, stabilization, and service coordination in order to de-escalate crisis ... Participates in agency-wide and departmental clinical research, as needed. * Participates in ...

Clinical Therapist I

Toledo, OH · On-site

$58.10K - $78.20K/yr

Provide crisis assessments, stabilization, and service coordination in order to de-escalate crisis ... Participates in agency-wide and departmental clinical research, as needed. * Participates in ...

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Clinical Research Coordinator information

See Toledo, OH salary details

$13

$25

$37

How much do clinical research coordinator jobs pay per hour?

As of May 28, 2026, the average hourly pay for clinical research coordinator in Toledo, OH is $25.66, according to ZipRecruiter salary data. Most workers in this role earn between $20.87 and $27.74 per hour, depending on experience, location, and employer.

What Is a Clinical Research Coordinator?

As a clinical research coordinator, your responsibilities and duties include overseeing research volunteers during medical trials for new drugs and medical devices. You train the volunteers and educate them about the trial and the rules they must follow. You also record data that they report and ensure they are doing the research ethically. Your job is to work with trial subjects, oversee the administration of medication or device usage, and conduct data collection accurately so that the results are as sound as possible. You must also report any unethical practices or concerns regarding trial volunteers to the doctors doing this research.

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

To thrive as a Clinical Research Coordinator, you need strong organizational abilities, attention to detail, and knowledge of clinical trial processes, often supported by a degree in life sciences or healthcare. Familiarity with regulatory compliance systems (such as GCP), electronic data capture (EDC) tools, and certifications like ACRP or SOCRA are typically required. Excellent communication, problem-solving, and teamwork skills enable effective coordination among investigators, sponsors, and patients. These competencies are crucial for maintaining data integrity, ensuring regulatory adherence, and supporting the overall success of clinical research studies.

What are some common challenges faced by Clinical Research Coordinators when managing multiple studies simultaneously?

Clinical Research Coordinators often manage several studies at once, which can present challenges in balancing timelines, documentation, and communication with various stakeholders. Keeping track of regulatory requirements, participant schedules, and data integrity for each study requires strong organizational skills and adaptability. Coordinators frequently collaborate with investigators, sponsors, and clinical staff to ensure protocol adherence and resolve issues quickly, making effective multitasking and prioritization essential to success in this role.

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

AspectClinical Research CoordinatorClinical Research Associate
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are commonOften requires a bachelor's or master's degree; certifications like CCRP or RAC are advantageous
Work EnvironmentWorks primarily at research sites, hospitals, or clinicsWorks mainly at sponsor offices, CROs, or monitoring sites
Employer & IndustryResearch institutions, hospitals, clinicsPharmaceutical companies, CROs, biotech firms
Job FocusManages daily study activities, patient recruitment, data collectionMonitors study progress, ensures compliance, verifies data accuracy

While both roles support clinical trials, Clinical Research Coordinators handle on-site study management and patient interactions, whereas Clinical Research Associates focus on monitoring and compliance from a remote or office setting. Understanding these differences helps in choosing the right career path or job search focus.

What are the most commonly searched types of Clinical Research jobs in Toledo, OH? The most popular types of Clinical Research jobs in Toledo, OH are:
What job categories do people searching Clinical Research Coordinator jobs in Toledo, OH look for? The top searched job categories for Clinical Research Coordinator jobs in Toledo, OH are:
What cities near Toledo, OH are hiring for Clinical Research Coordinator jobs? Cities near Toledo, OH with the most Clinical Research Coordinator job openings:
Infographic showing various Clinical Research Coordinator job openings in Toledo, OH as of May 2026, with employment types broken down into 67% Full Time, and 33% Part Time. Highlights an 100% In-person job distribution, with an average salary of $53,368 per year, or $25.7 per hour.
Clinical Research HRPP Program Specialist

Clinical Research HRPP Program Specialist

The University of Toledo

Toledo, OH • On-site

Full-time

Posted 12 days ago


University Of Toledo rating

6.4

Company rating: 6.4 out of 10

Based on 25 frontline employees who took The Breakroom Quiz

448th of 528 rated colleges and universities


Job description

Clinical Research HRPP Program Specialist
Job no: 500310
Work type: Staff - Full-Time
Location: Health Science Campus College Toledo, OH
Categories: Administration, Healthcare Positions, Hospital Administration, Full-Time, Research, None, Academic, Administrative Support
Title: Clinical Research HRPP Program Specialist
Department Org: Jacobson Clinical Research Center - 107980
Employee Classification: U1 - Unclassified PSA FT
Bargaining Unit: Professional Staff Association
Primary Location: MC AD
Shift: 1
Posted Salary: Salary will commensurate with experience
Job Description:
This role serves as a lead for monitoring regulations and guidance to identify and ensure implementation of changes to operational processes or best practices for clinical research. This position provides expert advice to principal investigators (PIs), Clinical Research Coordinators, leadership and other ORSP personnel involved in ensuring compliance throughout the lifecycle of clinical research and trials.
Responsible for the ongoing education and training of clinical research personnel and on-site clinical research monitoring of industry funded and investigator-initiated clinical research studies within the institution. Quality management duties include development and ongoing review of standard operating procedures (SOPs) and training documents for new coordinators that adheres to Good Clinical Practice (GCPs) and all applicable regulations.
Minimum Qualifications:
Requires Bachelor's in nursing, public health, healthcare, clinical research, or a related discipline.
• Minimum of four (4) years demonstrated professional and functionally relevant experience in an academic or regulatory setting as well as clinical research and trials. Including, but not limited to, human subject research, research processes, and compliance with appropriate regulations.
• Demonstrated experience in direct or indirect management or training of personnel.
• Knowledge of academic medical center standard practices and policies, including but not limited to Medicare Coverage Analysis, Fair Market Value and Standard of Care.
• Working knowledge of FDA and Good Clinical Practice guidelines and regulations
• Understanding of medical coding and knowledge of medical terminology
• Proficient in electronic health information systems (i.e., EPIC), Microsoft Office suite, and ability to learn and use other software systems as required by the position.
• Ability to define problems, collect data, establish facts, and draw valid conclusions.
• Background with federal and non-federal regulations for grant and contract management
Conditions of Employment:
To promote the highest levels of health and well-being, the University of Toledo campuses are tobacco-free. To further this effort, the University of Toledo Health Science Campus Medical Center is requiring candidates for employment to be nicotine-free. Pre-employment health screening requirements will include cotinine (nicotine) testing, as well as drug and other required health screenings for the position. With the exception of positions within University of Toledo Main Campus and the University of Toledo College of Medicine and Life Sciences, the employment offer is conditional upon successful completion of a cotinine test and Occupational Health clearance.
Equal Employment Opportunity Statement:
The University of Toledo is an equal opportunity employer. The University of Toledo does not discriminate in employment, educational programs, or activities on the basis of race, color, religion, sex, age, ancestry, national origin, sexual orientation, gender identity and expression, military or veteran status, disability, familial status, or political affiliation.
The University is dedicated to attracting and retaining the best and brightest talent and fostering a culture of respect.
The University of Toledo provides reasonable accommodation to individuals with disabilities. If you require accommodation to complete this application, or for testing or interviewing, please contact the HR Compliance at hrcompliance@utoledo.edu or 419-530-4747 between the hours of 8:30 a.m. and 5:00 p.m. or apply online for an accommodation request.
Computer access is available at most public libraries and at the Office of Human Resources located in the Center for Administrative Support on the Main Campus of the University of Toledo.
Advertised: 17 Dec 2025 Eastern Standard Time
Applications close:
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