Clinical Research Manager Jobs in Cincinnati, OH
Clinical Research Manager jobs in Cincinnati are concentrated in the Medical Center district, Kenwood, and the Clifton corridor, across academic medical centers, contract research organizations, and life sciences firms, with Cincinnati Children's Hospital, Medpace, and Velocity Clinical Research among those actively hiring. Demand is steady, driven by Cincinnati's dense cluster of hospital systems and pharma-adjacent employers. Scan the live roles below and apply to whichever ones fit.
Find JobsOverview
Open roles72
Top employerCincinnati Children's Hospital
Work type100% On-site
Top credentialBLS Certification
Companies hiring6
Showing 5 of 72+ Clinical Research Manager 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.
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Find JobsClinical Research Manager 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 Manager Jobs in Cincinnati: Frequently Asked Questions
How do I get a clinical research manager job in Cincinnati?
Focus on Cincinnati's academic medical centers, hospital-affiliated research institutes, and the contract research organizations clustered near the Medical Center and Kenwood corridors. Hands-on trial coordination experience, familiarity with FDA regulatory submissions, and a CCRP or CCRN credential give candidates a clear edge locally. Employers here tend to favor candidates who have managed multi-site studies and can work directly with principal investigators and IRB staff.
Which companies hire clinical research managers in Cincinnati?
Cincinnati clinical research manager roles are posted by Cincinnati Children's Hospital, Medpace, and Velocity Clinical Research and others right now, based on current listings on Migrate Mate as of September 2026. Hiring is spread across large academic health systems, regional hospital networks, and CROs that maintain Cincinnati offices to support ongoing pharmaceutical and device trials.
Are there remote clinical research manager jobs in Cincinnati?
Yes, though partially: clinical research manager work that involves site oversight, patient interaction, or on-site audit coordination is largely on-site by nature, while regulatory operations, data management, and sponsor-facing functions can often run remotely. About 0% of clinical research manager openings tied to Cincinnati are remote or hybrid as of September 2026, with hybrid arrangements most common at CROs and sponsor companies headquartered in or near the city.
How can I get a clinical research manager job in Cincinnati with little or no experience?
The most direct entry path in Cincinnati is through a clinical research coordinator role at one of the city's hospital systems or university-affiliated research programs, where coordinators gain the trial management and regulatory experience that managers are expected to hold. Cincinnati's academic medical centers and regional CROs regularly hire coordinators and research associates as stepping-stone roles, and a SOCRA or ACRP certification strengthens an early-career application significantly in this market.
Which industries hire the most clinical research managers in Cincinnati?
Cincinnati clinical research manager roles concentrate in Healthcare & Medical Services, Biotechnology & Pharmaceuticals, and Science & Research, based on current listings on Migrate Mate as of September 2026. Cincinnati's combination of major hospital systems, a long-standing consumer health and pharmaceutical presence, and growing device and biotech activity creates layered demand across all three sectors.
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