Top 15 Clinical study manager Jobs in Cincinnati, Oh

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 Associate II
AtriCure —Mason, OH
- $85,000 - $105,000 a year
- Remote
- Background check
- Anatomy knowledge
- Microsoft Excel
- Paid parental leave
- Health insurance
Manager, Clinical Operations
Meridian Bioscience, Inc. —Cincinnati, OH
- Full-time
- 5 years
- Bachelor of Science
- Master's degree
11d
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
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 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 QA Specialist - Pulmonary
Cincinnati Children's Hospital —Cincinnati, OH
- $56,846.40 - $72,488.00 a year
- Full-time
- Mid-level
- Bachelor's degree
- Children
Senior Clinical Research Associate (level dependent on experience)
CTI Clinical Trial Services, Inc —Covington, KY
- Hybrid work
- Nursing
- Mid-level
- Master's degree
- Paid parental leave
- Tuition reimbursement
Quick Apply
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
Clinical Research Coordinator II/III - Allergy - Devonshire Lab
Cincinnati Children's Hospital —Cincinnati, OH
- $24.46 - $26.23 an hour
- Full-time
- Mid-level
- Master's degree
- High school diploma or GED
Clinical Database Programmer
Medpace, Inc. —Cincinnati, OH
- Full-time
- Computer Science
- Office
- Bachelor's degree
- Free parking
- Health insurance
Logistics Team Lead - Study Setup
Thermo Fisher Scientific —Highland Heights, KY
- Online Application
- Hybrid work
- Background check
- Pass drug screening
- Mid-level
Clinical Research RN - MOB Lindner Research HV - Full Time - Days
The Christ Hospital Health Network —Cincinnati, OH
- Weekends as needed
- Nursing
- Patient monitoring
- RN License
1d
Director, ASL Central & Pediatric MR
GE HEALTHCARE —Cincinnati, OH
- Hybrid work
- 5 years
- Pass drug screening
- English
- Relocation assistance
- Health insurance

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Clinical Research Associate II
AtriCure —Mason, OH
Bachelor's degree in a science or related technical field required or demonstrated equivalent combination of education, training and experience.
$85,000 - $105,000 a year
Manager, Clinical Operations
Meridian Bioscience, Inc. —Cincinnati, OH
Lead Clinical Operations level initiatives for the development, maintenance and implementation of processes, tools, templates and plans.
11d

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Complete database query reviews for study candidacy and conduct outbound calls for study interest. Return all phone calls/email responses to interested patients…
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Clinical Research Coordinator IV - Bone Marrow Transplantation

Cincinnati Children's Hospital -
Cincinnati, OH

Apply Now

Job Details

Full-time
$61,401.60 - $78,291.20 a year

Qualifications

Laboratory sample storage
Project reporting
Data quality checks
Correspondence management
CCRC
Data storage
Clinical study protocols and reports
Database systems
Research ethical considerations
Project documentation
Medical statistical report preparation
Clinical research audit management
Data quality assurance
Records storage
Filing
Trend analysis
Master's degree
Collaborative research
Clinical audit and monitoring
Research report preparation
Collecting samples for laboratory testing
Bachelor's degree
Clinical data entry
Team management
Clinical training
Data quality monitoring
Clinical program data analysis
Managing clinical research teams
Clinical trial standard operating procedures
Implementing research protocols

Full Job Description

JOB RESPONSIBILITIES

Study Conduct/ Clinical Research Practice - Serve as a resource for others for all aspects of conducting a clinical trial for complex and multi-center trials. Develop & implement associated projects related to studies under the guidance of the principal investigator. Collaborate effectively with others to ensure proper progress & completion of studies. Assist other members by educating, providing resources, & consulting on difficult protocols or projects. Indirectly (or directly) supervise other CRCs. Train new staff in preparation & conduct of clinical trials. Provide oversight and guidance as needed to research staff. Collaborate on multiple projects or studies, and support other staff or the work flow involved in research work. Provide oversight and guidance to research staff for all aspects of conducting a clinical trial for complex and multi-center trials. Collect and process specimens to meet study requirements. Work with other divisions as needed to ensure proper handling, processing, storage and tracking of specimens per study requirements.

Regulatory Compliance and Documentation - Coordinate complex regulatory activities & periodic internal self-audit of records. May lead staff in regulatory activities. Provide oversight for the preparation, review, submission and maintenance of regulatory activities/submissions, ensure accuracy and timeliness to all collaborative parties. Provide oversight and guidance for project procurements. Coordinate and participate in monitor visits, audits, and quality reviews (internal and external) in a professional manner. Organize the review, correspondence and approval of human research protocols with all regulatory authorities, including study closeout. Determine which research protocols or issues have additional requirements, i.e. review by additional CCHMC Divisions, regulatory agencies, or consultants, and coordinate the process to meet these requirements. Act as a resource for regulatory affairs. Apply federal regulations; state and local law; and CCHMC and division policies and standard operating procedures (SOPs) to promote ethical practices in research involving human participants and to ensure compliance to those regulations. Ensure the documentation of regulatory activities in appropriate systems. Coordinate and maintain up-to-date and accurate written and electronic records and files.

Recruitment/Enrollment/Retention - Prepare study staff for recruitment/enrollment for medium to large/complex complexity projects. Oversee study staff performance. Proactively take initiative to ensure recruitment stays on track with the project time-lines. Implement successful plan to identify potential participants. Engage study staff to assist in identifying and enrolling participants. Proactively identify and monitor barriers to recruitment and problem-solve or innovate to overcome them. Determine best method/s to identify potential participants for research protocol (advertisements, chart reviews, monitoring of clinic schedule, etc.) and prepare accordingly. Create and maintain a detailed tracking system for participants considered for enrollment. Track progress at regular intervals and report out to PI and or management.

Data Management - Oversee data entry and validation to ensure accuracy, quality and compliance of data collection process. Create case report forms (CRFs) in consultation with other team members, as needed, using existing study data information to promote efficient data collection and data entry. Create Data Dictionary, as per protocol and in conjunction with principal investigator and statistician. Support the data-management process for clinical research projects, including addressing data queries from data managers, project statistician, and sponsors. Maintain and audit data, providing status and activity reports as required. Organize data to analyze, identify, and report trends. Review reports, tables, and listings. Assist in data analysis and maintain record keeping and data storage for clinical research studies. Maintain master database files for clinical research protocols. Prepare reports from validation studies of clinical research projects. Evaluate and resolve issues regarding contents of reports. Ensure quality of data submitted from study sites and assure timely submission of data. Oversee the processing of laboratory and other external data.

JOB QUALIFICATIONS

Bachelor's degree in a related field AND 3+ years of experience in related job discipline OR Master's degree and 2 years experience

Certified Clinical Research Coordinator within 18 months of external hire (SOCRA or ASCP)

Primary Location Burnet Campus

Schedule Full time

Shift Day (United States of America)

Department Bone Marrow Transplantation

Employee Status Regular

FTE 1

Weekly Hours 40

Expected Starting Pay Range *Annualized pay may vary based on FTE status $61,401.60 - $78,291.20

About Us

At Cincinnati Children’s, we come to work with one goal: to make children’s health better. We believe in a holistic team approach, both in caring for patients and their families, and in advancing science and discovery. We strive to do better and find energy and inspiration in our shared purpose. If you want to be the best you can be, you can do it at Cincinnati Children’s.

Cincinnati Children's is:
Recognized by U.S. News & World Report as a top 10 best Children's Hospitals in the nation for more than 15 years

Consistently among the top 3 Children's Hospitals for National Institutes of Health (NIH) Funding

Recognized as one of America’s Best Large Employers (2025) , America’s Best Employers for New Grads (2025)

One of the nation's America’s Most Innovative Companies as noted by Fortune

Consistently certified as great place to work

A Leading Disability Employer as noted by the National Organization on Disability

Magnet® designated for the fourth consecutive time by the American Nurses Credentialing Center (ANCC)

 We Embrace Innovation—Together. We believe in empowering our teams with the tools that help us work smarter and care better. That’s why we support the responsible use of artificial intelligence. By encouraging innovation, we’re creating space for new ideas, better outcomes, and a stronger future—for all of us.

Comprehensive job description provided upon request.

Cincinnati Children’s is proud to be an Equal Opportunity Employer committed to creating an environment of dignity and respect for all our employees, patients, and families. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, genetic information, national origin, sexual orientation, gender identity, disability or protected veteran status. EEO/Veteran/Disability

Apply Now

Refine Your Search

clinical study manager jobs in cincinnati, oh

Clinical Research Coordinator IV - Bone Marrow Transplantation

Clinical Research Associate II

Manager, Clinical Operations

Clinical Research Coordinator III

Clinical Research Coordinator III - Mayerson Center

Clinical Research Coordinator III - Bone Marrow Transplantation

Clinical Research QA Specialist - Pulmonary

Senior Clinical Research Associate (level dependent on experience)

Clinical Research Coordinator II/III - Hospital Medicine

Clinical Research Coordinator II/III - Allergy - Devonshire Lab

Clinical Database Programmer

Logistics Team Lead - Study Setup

Clinical Research RN - MOB Lindner Research HV - Full Time - Days

Director, ASL Central & Pediatric MR

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