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Clinical Project Manager Jobs in Ohio (NOW HIRING)

Medpace, Inc.

Clinical Project Coordinator

Cincinnati, OH · On-site

  • Medical

  • Retirement

  • PTO

In this role, you will work directly with Project Managers to support the day to day activities of Phase I clinical trials. If you are looking for a fast paced, collaborative work environment, then ...

Medpace, Inc.

Clinical Project Coordinator

Cincinnati, OH · On-site +1

  • Medical

  • Retirement

  • PTO

In this role, you will work directly with Project Managers to support the day to day activities of Phase I clinical trials. If you are looking for a fast paced, collaborative work environment, then ...

Medpace, Inc.

Study Start-Up Project Manager

Cincinnati, OH · On-site

  • Medical

  • Retirement

  • PTO

Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Study Start-Up Project Manager to join our Site Activation and Maintenance team. This position plays ...

Medpace, Inc.

Study Start-Up Project Manager

Cincinnati, OH · On-site +1

  • Medical

  • Retirement

  • PTO

Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Study Start-Up Project Manager to join our Site Activation and Maintenance team. This position plays ...

UC Health

Project Manager

Cincinnati, OH · On-site

At UC Health, we're proud to have the best and brightest teams and clinicians collaborating toward ... Minimum of 3-5 years of experience in a related project management position * Certified Healthcare ...

UC Health

Project Manager

Cincinnati, OH · On-site

Clinical/ Non-clinical Domain Project Management: Works with the departmental team and other ... departments (eg. Nursing, Support Services, etc.) to define projects and set the project scope ...

Managed Staffing

Junior Project Manager

Columbus, OH · On-site

$47 - $48/hr

Project Manager (Non-Clinical - Administrative) Location: Columbus, OH 43210 Shift: Day, 5x8 (08:00 AM - 05:00 PM) Position Overview Seeking a Junior Project Manager to support the planning and ...

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All JobsClinical Project JobsClinical Project Manager JobsClinical Project Manager Jobs in Ohio

Clinical Project Manager information

See Ohio salary details

$27

$57

$103

How much do clinical project manager jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for clinical project manager in Ohio is $57.71, according to ZipRecruiter salary data. Most workers in this role earn between $40.24 and $67.64 per hour, depending on experience, location, and employer.

How much do clinical project managers earn?

Clinical project managers typically earn between $80,000 and $130,000 annually, depending on experience, location, and the size of the organization. Senior roles or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. Compensation may also include bonuses and benefits related to project scope and complexity.

What is the difference between Clinical Project Manager vs Clinical Research Associate?

AspectClinical Project ManagerClinical Research Associate
CredentialsTypically requires a Bachelor's degree in life sciences, with many holding advanced degrees or certifications like PMPUsually holds a Bachelor's degree in life sciences or related field; certifications like CRA certification are common
Work EnvironmentManages multiple clinical trials, oversees teams, and coordinates with sponsors and sitesMonitors clinical sites, ensures protocol compliance, and collects data
Employer & Industry UsageFound in pharmaceutical, biotech, and CRO companies overseeing entire projectsPrimarily employed by CROs and sponsors to monitor trial sites

The Clinical Project Manager and Clinical Research Associate roles are closely related but differ mainly in scope. The Clinical Project Manager oversees entire clinical trials, manages teams, and coordinates with stakeholders, while the Clinical Research Associate focuses on monitoring clinical sites and ensuring protocol adherence. Both roles require similar educational backgrounds and certifications, but their responsibilities and work environments differ significantly.

What does a clinical project manager do?

A clinical project manager, or CPM, manages clinical trial studies for new drugs and medical devices. In this clinical management position, responsibilities and duties include working with all team members and all aspects of a clinical project, including subject selection and enrollment, record keeping, process auditing, and documentation. They also work with the budget and communicate with third parties, such as laboratories or investigators.

What are the key skills and qualifications needed to thrive as a clinical project manager, and why are they important?

To thrive as a Clinical Project Manager, you need expertise in clinical trial management, regulatory compliance, and a relevant life sciences degree, often supported by experience in clinical research. Familiarity with project management tools, electronic data capture (EDC) systems, and certifications like PMP or ACRP are highly valued. Strong leadership, problem-solving, and communication skills help you effectively coordinate teams and stakeholders. These competencies ensure successful trial execution, regulatory adherence, and timely project delivery in a highly regulated environment.

What does a clinical project manager do?

A Clinical Project Manager oversees the planning, execution, and completion of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They coordinate teams, manage budgets, timelines, and ensure that studies comply with regulatory standards and company protocols. Clinical Project Managers act as the main point of contact between sponsors, vendors, and clinical research sites, working to ensure that trials progress smoothly and data integrity is maintained. Their role is critical in bringing new therapies and treatments to market safely and efficiently.

What are some common challenges clinical project managers face when coordinating multi-site clinical trials?

Clinical Project Managers often encounter challenges such as maintaining consistent communication across different sites, ensuring adherence to regulatory guidelines, and managing timelines amidst unexpected delays. Coordinating multi-site trials requires balancing the needs of diverse teams, addressing site-specific issues, and ensuring data quality across all locations. Effective project management tools, regular status meetings, and proactive risk assessment are essential for overcoming these obstacles and keeping the study on track.
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What are the most commonly searched types of Clinical Project jobs in Ohio?

The most popular types of Clinical Project jobs in Ohio are:

What are popular job titles related to Clinical Project Manager jobs in Ohio?

For Clinical Project Manager jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Clinical Project Manager jobs in Ohio look for?

The top searched job categories for Clinical Project Manager jobs in Ohio are:

What cities in Ohio are hiring for Clinical Project Manager jobs?

Cities in Ohio with the most Clinical Project Manager job openings:

Clinical Project Manager jobs near you
Infographic showing various Clinical Project Manager job openings in Ohio as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 10% Part Time, and 4% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $120,036 per year, or $57.7 per hour.

Clinical Project Manager-Reference Laboratory

Medpace, Inc.

Cincinnati, OH • On-site

Other

Medical, Retirement, PTO

Re-posted 7 days ago

Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

13th of 73 rated research

Job description

Job Summary
We are currently seeking a Laboratory Project Manager for Medpace Reference Laboratories. This position is responsible for managing projects independently for one or more of Medpace Reference Laboratories' major clients.
Responsibilities
  • Supervise all aspects of designated clinical protocol with accountability of meeting agreed timelines, budgets, and performance quality;
  • Create and maintain laboratory manuals (general and study-specific) and other study- related documents;
  • Develop and present clinical laboratory presentations at investigator meetings;
  • Design specifications and monitor production of specimen collection kits;
  • Serve as primary contact for Sponsors regarding all aspects of assigned protocol(s);
  • Track study status as appropriate;
  • Communicate all aspects of protocol to various internal departments for appropriate study setup, maintenance, and closeout; and
  • Write, establish, and revise relevant Standard Operating Procedures and/or work instructions.

Qualifications
  • Bachelor's degree in science or a health-related field;
  • Knowledge of Microsoft Office;
  • 2 - 3 years of clinical laboratory experience;
  • 2 year project management experience required and;
  • Must have excellent oral and written communication skills

Travel: Up to 10%
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture
    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development
    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits
    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events and intramural sports

Cincinnati Headquarters Experience
    • A modern corporate campus designed to support collaboration and productivity
    • Multiple on-site dining options in the heart of Madison Square
    • Free on-site parking
    • Convenient access to on-site 24-7 fitness and wellness facilities

What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

What Medpace employees say

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About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992

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