Clinical Trial Manager Jobs in Ohio
Clinical Trial Manager jobs in Ohio are consistently active, with demand concentrated in pharmaceutical research, academic medical centers, and contract research organizations at levels from entry-level clinical trial coordinator through senior trial manager. Columbus, Cleveland, and Cincinnati anchor most of the hiring, where employers like Nationwide Children's Hospital, Cleveland Clinic, and Procter & Gamble have long-standing clinical development operations. The most in-demand specialties are oncology trials, Phase II through IV study management, and regulatory compliance oversight. Find a role that fits below and apply directly.
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Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers and Project Managers with a focus on Infectious Diseases to join our Clinical Trial Management Group at our Cincinnati, OH office. We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.
Responsibilities
- Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations;
- Serve as primary Sponsor contact for operational project-specific issues and study deliverables;
- Maintain in depth knowledge of protocol, therapeutic area, and indication;
- Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided;
- Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable;
- Develop operational project plans;
- Manage risk assessment and execution;
- Responsible for management of study vendor; and
- Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables.
BASIC QUALIFICATIONS
- Bachelor’s degree in a health-related field; Advanced degree in a health-related field preferred;
- Experience in Phases 1-4; Phases 2-3 preferred;
- 3-5 years as a project/clinical trial manager within a CRO;
- Management of overall project timeline; and
- Strong leadership skills.
ABOUT MEDPACE
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
WHY MEDPACE?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
CINCINNATI PERKS
- Cincinnati Campus Overview
- Flexible work environment
- Competitive PTO packages, starting at 20+ days
- Competitive compensation and benefits package
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
- Community involvement with local nonprofit organizations
- Discounts on local sports games, fitness gyms and attractions
- Modern, ecofriendly campus with an on-site fitness center
- Structured career paths with opportunities for professional growth
- Discounted tuition for UC online programs
AWARDS
- Named a Top Workplace in 2024 by The Cincinnati Enquirer
- Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
WHAT TO EXPECT NEXT
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
INTRODUCTION
Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers and Project Managers with a focus on Infectious Diseases to join our Clinical Trial Management Group at our Cincinnati, OH office. We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.
Responsibilities
- Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations;
- Serve as primary Sponsor contact for operational project-specific issues and study deliverables;
- Maintain in depth knowledge of protocol, therapeutic area, and indication;
- Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided;
- Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable;
- Develop operational project plans;
- Manage risk assessment and execution;
- Responsible for management of study vendor; and
- Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables.
BASIC QUALIFICATIONS
- Bachelor’s degree in a health-related field; Advanced degree in a health-related field preferred;
- Experience in Phases 1-4; Phases 2-3 preferred;
- 3-5 years as a project/clinical trial manager within a CRO;
- Management of overall project timeline; and
- Strong leadership skills.
ABOUT MEDPACE
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
WHY MEDPACE?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
CINCINNATI PERKS
- Cincinnati Campus Overview
- Flexible work environment
- Competitive PTO packages, starting at 20+ days
- Competitive compensation and benefits package
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
- Community involvement with local nonprofit organizations
- Discounts on local sports games, fitness gyms and attractions
- Modern, ecofriendly campus with an on-site fitness center
- Structured career paths with opportunities for professional growth
- Discounted tuition for UC online programs
AWARDS
- Named a Top Workplace in 2024 by The Cincinnati Enquirer
- Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
WHAT TO EXPECT NEXT
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
See All 5 Clinical Trial Manager Jobs in Ohio
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Find Clinical Trial Manager JobsClinical Trial Manager Jobs by City in Ohio
Where Ohio roles are concentrated, by current openings.
Clinical Trial Manager Job Market in Ohio
A snapshot from current Ohio openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Healthcare & Medical Services
- Biotechnology & Pharmaceuticals
What Ohio Employers Look For
The qualifications that appear most often in clinical trial manager jobs across Ohio.
- Bachelor's degree in life sciences, nursing, or a related clinical field required
- At least two years of clinical trial coordination or site management experience
- Working knowledge of ICH-GCP guidelines and FDA regulatory requirements
- Proficiency with clinical trial management systems such as Medidata Rave or Veeva Vault
- Strong project management skills with ability to manage multiple site timelines concurrently
- SOCRA or ACRP certification preferred by most Ohio research employers
Clinical Trial Manager Jobs in Ohio: Frequently Asked Questions
How do you become a clinical trial manager in Ohio?
Most clinical trial managers in Ohio begin with a bachelor's degree in a life science, nursing, or public health field, then spend several years working as a clinical trial coordinator or research associate at a hospital, CRO, or sponsor site. Ohio does not require a state-issued license specific to this role, but employers consistently favor candidates who hold a Certified Clinical Research Professional credential from SOCRA or a Certified Clinical Research Associate credential from ACRP before moving into management.
Which companies hire clinical trial managers in Ohio?
Employers hiring clinical trial managers in Ohio right now include Medpace, based on current listings on Migrate Mate as of August 2026. Ohio's strong concentration of academic medical centers, CROs, and pharmaceutical headquarters creates a broad range of opportunities across both sponsor-side and site-side management roles.
Which Ohio cities have the most clinical trial manager jobs?
Cincinnati account for the largest share of clinical trial manager openings in Ohio. Columbus draws the most postings because of its concentration of academic research hospitals and CRO offices, while Cleveland's strength in oncology and cardiovascular research at major health systems and Cincinnati's pharmaceutical and biotech industry base, anchored by long-established corporate research operations, keep both cities consistently active.
Are there remote clinical trial manager jobs in Ohio?
Yes, and more than many clinical roles, since trial managers spend a significant portion of their time on data review, vendor oversight, and regulatory documentation that can be done off-site. About 0% of clinical trial manager openings tied to Ohio are remote or hybrid as of August 2026, reflecting the desk-heavy nature of study oversight work. Site monitoring visits and investigator meetings still require travel, so fully remote roles typically focus on central monitoring or sponsor-side functions rather than hands-on site management.
How can I get hired as a clinical trial manager in Ohio with little or no experience?
The most realistic entry path is a clinical trial coordinator or research associate role at one of Ohio's academic medical centers or large CRO offices, where you gain direct site-level trial experience before stepping into management. Nationwide Children's Hospital, Cleveland Clinic, and Ohio State University Wexner Medical Center all run research operations that regularly onboard early-career coordinators. A SOCRA or ACRP certification, even before your first coordinator role, signals commitment and gives your application an immediate edge in a competitive applicant pool.
Where can I find and apply to clinical trial manager jobs in Ohio?
You can find and apply to clinical trial manager jobs in Ohio on Migrate Mate, which lists current Ohio openings updated regularly. Search the listings, find roles that match your experience level and specialty, and apply directly to the ones that fit.
See All 5 Clinical Trial Manager Jobs in Ohio
Find roles in Ohio that match your experience and apply in just a few clicks.
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