Clinical Research Nurse Jobs in Cincinnati, OH
Clinical Research Nurse jobs in Cincinnati are concentrated in the medical corridor anchoring Avondale, Clifton, and the broader UC Health campus area, with strong demand from oncology, cardiovascular, and neurology trial units at employers including Cincinnati Children's Hospital, Medpace, and Velocity Clinical Research. Cincinnati's dense cluster of academic medical centers and independent research sites keeps hiring active year-round. Scan the live roles below and apply to whichever ones fit.
Find Clinical Research Nurse JobsOverview
Open roles72
Top employerCincinnati Children's Hospital
Work type100% On-site
Top credentialBLS Certification
Companies hiring6
Showing 5 of 72+ Clinical Research Nurse jobs
Clinical Research Assistant
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Added 1d ago
Velocity Clinical Research, Inc.
Clinical Research Assistant
Cincinnati, Ohio
Added 1d ago
Clinical Research Coordinator I
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Added 1d ago
Velocity Clinical Research, Inc.
Clinical Research Coordinator I
Cincinnati, Ohio
Added 1d ago
Lead Research Data Scientist - Multimodal Clinical Data
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Added 2d ago
Cincinnati Children's Hospital
Lead Research Data Scientist - Multimodal Clinical Data
Cincinnati, Ohio
Added 2d ago
Neonatology - Clinical & Research Opportunities
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Added 6d ago
Cincinnati Children's Hospital
Neonatology - Clinical & Research Opportunities
Cincinnati, Ohio
Added 6d ago
Clinical Research Coordinator III/IV - Bone Marrow Transplantation
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Added 1w ago
Cincinnati Children's Hospital
Clinical Research Coordinator III/IV - Bone Marrow Transplantation
Cincinnati, Ohio
Added 1w ago
Added 1d ago
Clinical Research Assistant
Velocity Clinical Research, Inc.·Cincinnati, Ohio
Job functions:
On-Site
High school diploma or GED
201-500 employees
Job Description
Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step.
As an employee of Velocity, you are the most integral part of our mission. For talented candidates who perform at a high level, Velocity will invest to support career advancement and reward performance. Whether you are new to clinical research or are an industry veteran, we invite you to apply to Velocity.
Benefits include medical, dental and vision insurance, paid time off and company holidays, 401(k) retirement plan with company-match, and an annual incentive program.
Summary:
The Clinical Research Assistant assists the Clinical Operations Team in a multi-functional capacity to carry out all assigned tasks associated with the collection, documentation, and maintenance of clinical data including phlebotomy/laboratory, data entry and administrative responsibilities.
Duties/Responsibilities:
- Assist in the conduct of clinical trials in accordance with the study protocol, GCP, ICH Guidelines, and Velocity’s SOPs
- Perform venipuncture, capillary puncture and/or other fluid collection within scope of the protocol and local law and regulations
- With supervision, perform clinical assessments (vital signs, phlebotomy, ECG, etc) within scope of the protocol, local law and regulations
- Process, package and ship laboratory specimens as required per protocol and IATA regulations, if applicable
- Track, order and maintain inventory of all laboratory and study related supplies throughout course of the clinical trial
- Enter source data into the sponsor's and/or vendor’s data portal and resolve basic queries in a timely manner under the direction of the Clinical Research Coordinator
- Communicate with coworkers, leadership, study subjects, sponsors, CROs, and vendors under the direction of the Clinical Research Team
- Understand good documentation practices when collecting, transferring data to sponsor/CRO data capture systems and resolving queries under the direction of the Clinical Research Coordinator
- Understand the informed consent process with emphasis on ensuring initial and ongoing consent of study subjects
- Understand basic elements of regulatory documentation required to initiate, maintain and close a clinical research trial
- Understand and participate in patient recruiting tasks including but not limited to prescreening potential subjects for clinical research trials either via phone or in person
- Maintain confidentiality of patient protected health information, sponsor confidential information and Velocity confidential information
- Ability to escalate potential patient safety issues such as adverse events, serious adverse events, and adverse events of special interest to the Clinical Research Team
- Cleaning, organizing, and disinfecting the patient care, lab and lab equipment areas as needed
- Prepare source document charts, copy and/or file medical records and study related documents as required.
- Perform front office duties as needed including but not limited to answering phones, scheduling subjects, making reminder calls and updating patient tracking systems.
- Other duties as assigned
Education/Experience:
- High School Graduate and/or technical degree with minimum of 1 year of relevant experience in life sciences industry
Required Licenses/Certifications:
- Phlebotomy if applicable and required by state law
- Intramuscular dose administration and preparation if applicable and required by state law
Required Skills:
- Demonstrated knowledge of medical terminology
- Demonstrated ability to use the following technology: Computers, Microsoft Office software, fax, copier, and multi-line telephone.
- Understanding of verbal, written, and organizational skills
- Demonstrated ability to work as a team player
- Demonstrated ability to read, write, and speak English
- Demonstrated ability to multi-task
- Demonstrated ability to follow written guidelines
- Demonstrated ability to be flexible/adapt as daily schedule may change rapidly
Required Physical Abilities:
- Sit or stand for long periods of time
- Communicate in person and by a telephone
- Limited walking required
- Limited to lifting up to 30 pounds
NOTE: The above Job Description is intended to communicate the general function of the mentioned position and by no means should be considered an exhaustive or complete outline of the specific tasks and functions that will be required. Additionally, specific tasks and duties of the position are subject to change as the Company, the department and circumstances change. All employees are expected to perform their duties within their ability as required by the job and/or as requested by management.
Velocity Clinical Research, Inc.
Clinical Research Assistant
Cincinnati, Ohio
Added 1d ago201-500 employees
Job functions:
On-Site
High school diploma or GED
Job Description
Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step.
As an employee of Velocity, you are the most integral part of our mission. For talented candidates who perform at a high level, Velocity will invest to support career advancement and reward performance. Whether you are new to clinical research or are an industry veteran, we invite you to apply to Velocity.
Benefits include medical, dental and vision insurance, paid time off and company holidays, 401(k) retirement plan with company-match, and an annual incentive program.
Summary:
The Clinical Research Assistant assists the Clinical Operations Team in a multi-functional capacity to carry out all assigned tasks associated with the collection, documentation, and maintenance of clinical data including phlebotomy/laboratory, data entry and administrative responsibilities.
Duties/Responsibilities:
- Assist in the conduct of clinical trials in accordance with the study protocol, GCP, ICH Guidelines, and Velocity’s SOPs
- Perform venipuncture, capillary puncture and/or other fluid collection within scope of the protocol and local law and regulations
- With supervision, perform clinical assessments (vital signs, phlebotomy, ECG, etc) within scope of the protocol, local law and regulations
- Process, package and ship laboratory specimens as required per protocol and IATA regulations, if applicable
- Track, order and maintain inventory of all laboratory and study related supplies throughout course of the clinical trial
- Enter source data into the sponsor's and/or vendor’s data portal and resolve basic queries in a timely manner under the direction of the Clinical Research Coordinator
- Communicate with coworkers, leadership, study subjects, sponsors, CROs, and vendors under the direction of the Clinical Research Team
- Understand good documentation practices when collecting, transferring data to sponsor/CRO data capture systems and resolving queries under the direction of the Clinical Research Coordinator
- Understand the informed consent process with emphasis on ensuring initial and ongoing consent of study subjects
- Understand basic elements of regulatory documentation required to initiate, maintain and close a clinical research trial
- Understand and participate in patient recruiting tasks including but not limited to prescreening potential subjects for clinical research trials either via phone or in person
- Maintain confidentiality of patient protected health information, sponsor confidential information and Velocity confidential information
- Ability to escalate potential patient safety issues such as adverse events, serious adverse events, and adverse events of special interest to the Clinical Research Team
- Cleaning, organizing, and disinfecting the patient care, lab and lab equipment areas as needed
- Prepare source document charts, copy and/or file medical records and study related documents as required.
- Perform front office duties as needed including but not limited to answering phones, scheduling subjects, making reminder calls and updating patient tracking systems.
- Other duties as assigned
Education/Experience:
- High School Graduate and/or technical degree with minimum of 1 year of relevant experience in life sciences industry
Required Licenses/Certifications:
- Phlebotomy if applicable and required by state law
- Intramuscular dose administration and preparation if applicable and required by state law
Required Skills:
- Demonstrated knowledge of medical terminology
- Demonstrated ability to use the following technology: Computers, Microsoft Office software, fax, copier, and multi-line telephone.
- Understanding of verbal, written, and organizational skills
- Demonstrated ability to work as a team player
- Demonstrated ability to read, write, and speak English
- Demonstrated ability to multi-task
- Demonstrated ability to follow written guidelines
- Demonstrated ability to be flexible/adapt as daily schedule may change rapidly
Required Physical Abilities:
- Sit or stand for long periods of time
- Communicate in person and by a telephone
- Limited walking required
- Limited to lifting up to 30 pounds
NOTE: The above Job Description is intended to communicate the general function of the mentioned position and by no means should be considered an exhaustive or complete outline of the specific tasks and functions that will be required. Additionally, specific tasks and duties of the position are subject to change as the Company, the department and circumstances change. All employees are expected to perform their duties within their ability as required by the job and/or as requested by management.
See All 72 Clinical Research Nurse Jobs in Cincinnati
Find roles in Cincinnati that match your experience and apply in just a few clicks.
Find Clinical Research Nurse JobsClinical Research Nurse Job Market in Cincinnati
Who's Hiring
- Cincinnati Children's Hospital30
- Medpace15
- Velocity Clinical Research11
- The Christ Hospital Health Network8
- Science 374
Top Industries Hiring
- Healthcare & Medical Services15
- Biotechnology & Pharmaceuticals8
- Science & Research4
Clinical Research Nurse Jobs in Cincinnati: Frequently Asked Questions
How do I get a clinical research nurse job in Cincinnati?
Focus your search on Cincinnati's academic medical center corridor in Avondale and Clifton, where the heaviest concentration of phase II and III trials runs. Oncology and cardiovascular research units hire most actively, so tailor your resume toward protocol adherence, informed consent, and adverse event documentation. Candidates who hold CCRP certification or have recent experience with electronic data capture systems stand out in this market.
Which companies hire clinical research nurses in Cincinnati?
Companies currently hiring clinical research nurses in Cincinnati include Cincinnati Children's Hospital, Medpace, and Velocity Clinical Research, per current listings on Migrate Mate as of September 2026. Cincinnati's hiring pool is driven by large academic health systems, specialty hospital networks, and contract research organizations that support multi-site trials across the region.
Are there remote clinical research nurse jobs in Cincinnati?
Yes, though with limits, clinical research nursing is largely hands-on, so fully remote roles are uncommon, but hybrid arrangements exist for coordinators handling regulatory submissions, data queries, and sponsor communications. About 0% of clinical research nurse openings tied to Cincinnati are remote or hybrid as of September 2026. The most remote-compatible tasks in Cincinnati-based roles tend to be IRB documentation, protocol review, and study closeout activities.
How can I get a clinical research nurse job in Cincinnati with little or no experience?
The most realistic entry path in Cincinnati is moving laterally from a clinical bedside role, particularly in oncology or cardiology units at one of the city's large health systems, where research coordinators are often recruited internally. Research assistant and clinical trials coordinator roles at Cincinnati's contract research organizations offer another opening. Volunteering on an IRB committee or completing a Good Clinical Practice certification strengthens any entry-level application in this market.
Which industries hire the most clinical research nurses in Cincinnati?
Cincinnati clinical research nurse roles concentrate in Healthcare & Medical Services, Biotechnology & Pharmaceuticals, and Science & Research, based on current listings on Migrate Mate as of September 2026. Cincinnati's strong academic medical infrastructure, combined with a growing number of contract research organizations operating in the metro area, keeps those sectors consistently at the top of local hiring volume.
See All 72 Clinical Research Nurse Jobs in Cincinnati
Find roles in Cincinnati that match your experience and apply in just a few clicks.
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