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 Medpace, Cincinnati Children's Hospital, and The Christ Hospital Health Network. 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.
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Facilitates the start-up of clinical projects in an acute care/inpatient/outpatient setting. Assists in project initiation, which includes educating physicians and hospital staff, implementing study protocol assignments, facilitating patient enrollment and follow-up. Assures protocol compliance, reports to the study Sponsor, and coordinates study participation with the patient’s clinical health plan. The goal is to complete each clinical trial with required enrollment, retention of subjects, and accurate data in accordance with FDA guidelines. The RN will need to have a willingness to learn innovative procedures such as the preparation and administration of stem cells, the use of investigational devices and the administration of investigational medications.
1. Responsible for project management and implementation of study protocols.
- Assists in the initiation and maintenance of protocols. Strategically plans the study flow and creates outlines and source documents.
- Responsible for the training of research staff members, physicians and ancillary hospital healthcare professionals on study related procedures.
- Adjusts information aids, standing orders, study outlines when amendments to the protocols occur.
- Consents patients, verifies inclusion/exclusion criteria, facilitates testing and procedures, and coordinates patient visits to meet protocol requirements.
- Must be familiar with the policies and procedures of other hospital departments, i.e., OR, Cath Lab, EP Lab, ICU, ED, Cancer Center and telemetry units.
- Performs procedures and collects data in the ED, Cath Lab, EP Lab, ICU/step down area, physician office, O.R., Cancer Center and other required areas
- Assists physicians and ancillary hospital staff with procedures and data collection on sub-studies associated with project.
- Professionally represents the principal investigator and research center at Investigator Meetings and training sessions.
- Accurately maintains Case Report Forms (CRFs) and source documentation.
- Submits serious adverse events (SAEs) to the IRB and sponsor per established guidelines.
- Responsible for accountability during monitoring visits, sponsor audits, and FDA audits.
- Fulfills on call duties related to study procedures.
2. Coordinates project management and patient activities to provide compliance.
- Serves as the contact for physicians, nurses and other ancillary hospital staff to assure that all research and related clinical needs are achieved.
- Verifies that patients are scheduled appropriately for follow up evaluations per protocol guidelines.
- Responsible for educating patients on the scientific objectives of the study as well as to the importance of compliance with follow-up.
- Maintain control of drug/device inventory and validate storage at the appropriate temperature.
- Guides the primary care physician in facilitating good protocol compliance and clinical patient care through awareness of protocol objectives and design.
- Makes recommendations on how to facilitate special or acute needs of patients.
- Assists the screening team with patient consenting and performs reconsenting as necessary.
- Fulfills IRB/FDA and protocol expectations.
3. Facilitates and maintains high patient enrollment and participation in research protocols.
- Encourages new patient enrollment by identifying potential research patients, discussing the protocols with physicians and communicating this information to the screeners to facilitate the process.
- Works collaboratively with the physicians, hospital staff, patients, family, and study sponsors to implement research procedures to promote optimal outcomes.
- Alerts operational managers and physicians of possible patient withdrawal or continuance issues immediately in order to implement a plan that will encourage compliance with follow-up.
- Provides ongoing education to the patient and family members on the risks/benefits of the study in an effort to develop rapport and encourage compliance.
4. Participates directly in patient care duties associated with projects.
- Requires case management skills to assist the patient with financial aid in order to obtain medication, medical care or transportation.
- Possesses a diverse knowledge base and is proficient in critical care nursing skills and procedures.
- Continual assessment of patients to evaluate the outcomes of the use of the investigational drug/device.
- Maintains accurate awareness of all clinical projects within the research center.
- Utilizes critical thinking skills when executing protocol procedures to maintain patient safety.
- Guides the physician in protocol compliance while making recommendations on how to facilitate special or acute needs of the patient.
5. Performs other related duties as required or requested.
- Assures that the research center’s needs are recognized and cooperatively met and action is taken as required to obtain desired outcomes.
- Assists non-RN staff with any clinical tasks or decision making duties.
- On-call responsibilities as required that includes approximately one weekend every three months.
- Assists in training of new staff as needed.
- Demonstrates enthusiasm in the job.
KNOWLEDGE AND SKILLS:
Please describe any specialized knowledge or skills, which are REQUIRED to perform the position duties. Do not personalize the job description, credentials, or knowledge and skills based on the current associate. List any special education required for this position.
EDUCATION: RN Diploma degree or Associates in Nursing required, BSN preferred, BSN must be obtained within 5 years of date of hire.
YEARS OF EXPERIENCE: 3-5 years direct patient care experience required with 3 years clinical research and FDA/IRB regulations operations preferred.
REQUIRED SKILLS AND KNOWLEDGE: Photocopier, fax equipment, computer, all medical equipment appropriate to research, and strong organizational skills. Excellent communication skills, all essential patient care equipment and duty knowledge.
LICENSES & CERTIFICATIONS:
Licensed and Registered by the State of Ohio as a Registered Nurse.
Basic Life Support (BLS)
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Find Clinical Research Nurse JobsClinical Research Nurse Job Market in Cincinnati
Who's Hiring
- Medpace55

- Cincinnati Children's Hospital26

- The Christ Hospital Health Network7

- IQVIA3

- EmVenio Research3

Top Industries Hiring
- Science & Research46
- Healthcare & Medical Services23
- Biotechnology & Pharmaceuticals10
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 Medpace, Cincinnati Children's Hospital, and The Christ Hospital Health Network, per current listings on Migrate Mate as of August 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 21% of clinical research nurse openings tied to Cincinnati are remote or hybrid as of August 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 Science & Research, Healthcare & Medical Services, and Biotechnology & Pharmaceuticals, based on current listings on Migrate Mate as of August 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.
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