Top 55 Research coordinator Jobs in Ohio

Lead Travel Clinical Research Coordinator
The Clinical Trials Network, LLC —Sandusky, OH
- $60,000 - $80,000 a year
- Full-time
- Nursing
- Up to 50% travel
- Ability to walk for extended periods
- Health insurance
- 401(k)
Quick Apply
6d
Clinical Research Coordinator I
Nationwide Children's Hospital —Columbus, OH
- Weekends as needed
- Hospital
- Word processing
- Bachelor of Science
Clinical Research Coordinator
OhioHealth —Columbus, OH
- Full-time
- Mid-level
- Bachelor's degree
- Travel
Clinical Research Coordinator
Dayton Center For Neurological Disorders Inc —Centerville, OH
- $25 - $35 an hour
- Full-time
- RN License
- Medical office experience
- Mid-level
- Profit sharing
- Disability insurance
Clinical Research Coordinator II
Nationwide Children's Hospital —Columbus, OH
- Full-time
- Word processing
- Bachelor of Science
- Mid-level
Clinical Research Coordinator III - Mayerson Center
Cincinnati Children's Hospital —Cincinnati, OH
- $56,784.00 - $62,150.40 a year
- Full-time
- Mid-level
- Master's degree
- Bachelor's degree
Clinical Research Coordinator I
ObjectiveHealth —Springboro, OH
- Full-time
- Mid-level
- Clinic
- US work authorization
- Paid holidays
- Disability insurance
Quick Apply
2d
Clinical Research Coordinator III
Cincinnati Children's Hospital —Cincinnati, OH
- $56,784.00 - $62,150.40 a year
- Full-time
- Psychiatry
- Mid-level
- Master's degree
8d
Research Coordinator/Interventionist-1
Nationwide Children's Hospital —Columbus, OH
- Full-time
- Hospital
- Word processing
- Bachelor of Science
Clinical Research Coordinator
U.S. Renal Care —Alexis, OH
- $62,231 - $77,789 a year
- Microsoft Excel
- Microsoft Outlook
- Customer service
9h
Clinical Research Coordinator
Wright State University —Dayton, OH
- Vital signs
- Mid-level
- Bachelor's degree
Clinical Research Coordinator III - Bone Marrow Transplantation
Cincinnati Children's Hospital —Cincinnati, OH
- $56,784.00 - $62,150.40 a year
- Full-time
- Master's degree
- Bachelor's degree
- Children
Clinical Research Coordinator I - RI Behav Trials Off
Nationwide Children's Hospital —Columbus, OH
- Weekends as needed
- Hospital
- Word processing
- Writing skills
Newborn Screening Coordinator- Research Hematology
Nationwide Children's Hospital —Columbus, OH
- Full-time
- Mid-level
- Master's degree
- Bachelor's degree
Clinical Research Coordinator - Comprehensive Transplant Center
The Ohio State University Wexner Medical Center —Columbus, OH
- Weekends as needed
- Background check
- Patient monitoring
- Pass drug screening
6d
Clinical Research Coordinator IV - Bone Marrow Transplantation
Cincinnati Children's Hospital —Cincinnati, OH
- $61,401.60 - $78,291.20 a year
- Full-time
- Master's degree
- Bachelor's degree
- Team management
Clinical Research Study Coordinator
Intrepid Research —Cincinnati, OH
- $25 - $35 an hour
- Full-time
- Mid-level
- 3 years
- Bachelor's degree
- Health savings account
- Health insurance
Quick Apply
8d
Clinical Research Coordinator II/III - Hospital Medicine
Cincinnati Children's Hospital —Cincinnati, OH
- $24.46 - $26.23 an hour
- Full-time
- Mid-level
- Master's degree
- High school diploma or GED
Research Regulatory Coordinator - RI Pulmonary Med
Nationwide Children's Hospital —Columbus, OH
- Full-time
- Computer literacy
- Driving
- Experience equivalent to degree accepted
Clinical Research Coordinator II - RI Emergency Medicine
Nationwide Children's Hospital —Columbus, OH
- Full-time
- Word processing
- Bachelor of Science
- Mid-level

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Lead Travel Clinical Research Coordinator

The Clinical Trials Network, LLC
Sandusky, OH

Quick Apply

Job Details

Full-time
$60,000 - $80,000 a year
6 days ago

Benefits

Health insurance
401(k)
Paid time off
Opportunities for advancement
Life insurance

Qualifications

Clinical research methods
CCRC
Healthcare Administration
HIPAA
Research project coordination
ICH guidelines
Driver's License
Clinical research compliance
Bachelor's degree
Public Health
Clinical quality assurance standards
FDA regulations

Full Job Description

Position Summary

CTNx is seeking an experienced and highly motivated Travel Clinical Research Coordinator (CRC) to support an expanding clinical research program. This role is ideal for a research professional who enjoys working directly with patients, physicians, and study sponsors while helping build and support research operations across multiple clinical sites.

The Travel CRC will serve as the primary coordinator for assigned clinical trials and will be responsible for participant recruitment, study execution, regulatory compliance, source documentation, data collection, and sponsor communication. This individual will travel regularly to research locations, initial primary location being Sandusky, and other Ohio-based sites as research operations continue to expand (Lyndhurst, Lorain, etc).

The successful candidate will be highly organized, adaptable, self-motivated, and capable of working independently while maintaining the highest standards of patient care, data quality, and regulatory compliance.

Essential Duties and Responsibilities

Clinical Trial Management

Coordinate and manage clinical trials from study start-up through closeout.
Serve as the primary liaison between Principal Investigators, study sponsors, CROs, and CTNx leadership.
Ensure strict adherence to study protocols, sponsor requirements, and regulatory guidelines.
Track study milestones, enrollment goals, participant visits, and study deliverables.
Identify, document, and communicate protocol deviations and corrective actions.
Support monitoring visits, audits, and sponsor inspections.
Ensure participant safety through ongoing oversight and adverse event management.

Patient Recruitment and Retention

Identify and screen potential research participants according to protocol-defined inclusion and exclusion criteria.
Conduct informed consent discussions and ensure participants fully understand study requirements, risks, and benefits.
Develop and implement recruitment and retention strategies to meet enrollment goals.
Maintain consistent communication with study participants throughout the duration of the trial.
Coordinate participant scheduling and follow-up activities.
Address participant concerns and provide exceptional patient support.

Data Collection and Documentation

Maintain accurate, complete, and timely source documentation utilizing CRIO and sponsor-required systems.
Enter study data and resolve data queries within established timelines.
Document and report adverse events, serious adverse events, and protocol deviations.
Maintain audit-ready study files and essential regulatory documentation.
Ensure participant confidentiality and compliance with HIPAA requirements.
Support source document review and quality assurance activities.

Regulatory and Compliance Responsibilities

Maintain compliance with FDA regulations, ICH-GCP guidelines, sponsor requirements, and institutional policies.
Assist with preparation and submission of regulatory documentation to Institutional Review Boards (IRBs).
Ensure informed consent processes are conducted and documented appropriately.
Support regulatory inspections, sponsor audits, and internal quality reviews.
Maintain accurate delegation logs, training records, and study-specific documentation.
Ensure all research activities are conducted ethically and in accordance with applicable regulations.

Site Support and Travel Responsibilities

Travel regularly to research locations throughout northeast Ohio.
Provide on-site research coordination support during study start-up, enrollment, monitoring visits, and closeout activities.
Collaborate with physicians, practice staff, and CTNx operational teams to ensure successful study execution.
Assist in establishing and maintaining research workflows across multiple locations.
Support future site expansion initiatives as additional research locations are activated.
Backup coordination for CTNx clients as necessary

The above list of duties is intended to describe the general nature and level of work performed by individuals assigned to this position. It is not to be construed as an exhaustive list of duties performed by the individual so classified, nor is it intended to limit or modify the right of any supervisor to assign, direct, and control the work of employees under his/her supervision.

Required Qualifications

Bachelor's Degree in Life Sciences, Healthcare Administration, Nursing, Public Health, or related field.
Minimum of three (3) years of Clinical Research Coordinator experience.
Demonstrated experience coordinating industry-sponsored clinical trials.
Working knowledge of FDA regulations, ICH-GCP guidelines, and IRB processes.
Experience with electronic data capture systems and source documentation practices.
Strong organizational, communication, and problem-solving skills.
Ability to work independently in a fast-paced environment.
Valid driver's license and reliable transportation.

Preferred Qualifications

ACRP Certification (CCRC) and/or SOCRA Certification (CCRP).
Two (2) years as Lead/Senior Clinical Research Coordinator experience.
Experience working across multiple therapeutic areas.
Experience utilizing CRIO or similar clinical research source management platforms.
Experience supporting multi-site clinical research programs.
Previous experience working with physician-owned research sites.

Physical Requirements

Ability to travel frequently
Ability to sit, stand, and walk for extended periods.
Ability to transport research materials and equipment when necessary.
Ability to work on-site in clinical environments.

What We Offer

Competitive salary and performance-driven environment.
Opportunity to work alongside leading physicians and research professionals.
Exposure to diverse therapeutic areas and clinical trials.
Career growth opportunities within a rapidly expanding clinical research network.
Meaningful impact on advancing clinical research and improving patient care.

CTNx is an Equal Opportunity Employer and is committed to fostering a diverse and inclusive workplace.

Pay: $60,000.00 - $80,000.00 per year

Benefits:

401(k)
Health insurance
Life insurance
Paid time off

Experience:

Clinical Research Coordinator: 3 years (Required)

Location:

Sandusky, OH 44871 (Required)

Willingness to travel:

50% (Required)

Work Location: In person

Quick Apply

Refine Your Search

research coordinator jobs in ohio

Lead Travel Clinical Research Coordinator

Clinical Research Coordinator I

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Coordinator II

Clinical Research Coordinator III - Mayerson Center

Clinical Research Coordinator I

Clinical Research Coordinator III

Research Coordinator/Interventionist-1

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Coordinator III - Bone Marrow Transplantation

Clinical Research Coordinator I - RI Behav Trials Off

Newborn Screening Coordinator- Research Hematology

Clinical Research Coordinator - Comprehensive Transplant Center

Clinical Research Coordinator IV - Bone Marrow Transplantation

Clinical Research Study Coordinator

Clinical Research Coordinator II/III - Hospital Medicine

Research Regulatory Coordinator - RI Pulmonary Med

Clinical Research Coordinator II - RI Emergency Medicine

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