Clinical Project Manager Jobs in Ohio
Clinical Project Manager jobs in Ohio are in strong demand, with openings concentrated in pharmaceutical research, medical device development, and academic medical center trials at every level from associate project manager through senior and executive program roles. Columbus, Cleveland, and Cincinnati anchor most of the hiring, where employers like Cardinal Health, the Cleveland Clinic health system, and Nationwide Children's Hospital maintain consistent clinical operations and research pipelines. Therapeutic areas driving the most openings include oncology, cardiovascular, and rare disease trials. Find a role that fits below and apply directly.
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Showing 5 of 9+ Clinical Project Manager jobs
Oversees the administrative functions of single and/or multi-institutional research trials. Coordinates/Manages daily organization and operational issues/activities related to Phase I-IV clinical research trials. Facilitates key trial communications for academic coordination, provides clinical perspective to the design and conduct of clinical trials.
Join Cleveland Clinic Research, where you will work alongside passionate caregivers and make a lasting, meaningful impact on patient care. Here, you will receive endless support and appreciation while building a rewarding career with one of the most respected healthcare organizations in the world.
Groundbreaking discoveries happen every day at Cleveland Clinic. As a Clinical Research Project Manager, you will interact with various research teams and play a crucial role in managing the clinical research that allows Cleveland Clinic to continue to innovate and drive better outcomes for patients. Clinical research is the only way that medicine comes on the market, pushing the edge of moving medicine forward. Come join a culture devoted to pushing the needle forward in healthcare.
In Pediatric Hematology and Oncology you will support research and clinical trials for our youngest cancer patients. Learn more here
A caregiver in this role works days from 8:30am-5:00pm. Start/end times may vary.
A caregiver who excels in this role will:
Oversee the administrative functions of single and/or multi-institutional research trials.
Coordinate/manage daily organization and operational issues/activities related to Phase I-IV clinical research trials.
Facilitate key trial communications for academic coordination.
Provide clinical perspective to the design and conduct of clinical trials.
Manage and coordinate a clinical trials team (external industry team members, statisticians, database programmers and researchers) responsible for data accumulation, input and analysis.
Interact with the Finance and Legal Departments to facilitate clinical trial budget, site budget and contract execution.
Maintain professional relationships with sponsors, including frequent, open communication and associated documentation.
Coordinate development, preparation, review and approval of research protocols, case report forms and regulatory documents for the conduct of research required by Institutional Review Board (IRB), Sponsor and FDA.
Collect and review regulatory documents from sites.
Communicate with institutional and central IRBs, FDA and other parties regarding protocol subject and safety issues.
Organize, coordinate, attend and participate in Investigator Meetings and training programs.
Develop and maintain planned communication with sites (i.e., newsletters, study progress updates, telephone communication, supportive reinforcement of Sponsor communication, etc.).
Analyze site strengths and weaknesses related to intended protocol and selection of qualified investigators and sites.
Assess investigator and site performance.
Lead initiatives to improve quality and make recommendations to discontinue sites if necessary.
Assist with the development, implementation and evaluation of research subject recruitment strategies, including marketing strategies, to maximize enrollment and retention.
Complete training in Human Subjects Research (HSR) as required by the Responsible Conduct of Research guidelines adopted by the Cleveland Clinic.
Perform other duties as assigned.
Minimum qualifications for the ideal future caregiver include:
Bachelor’s Degree in Nursing, Science, Healthcare or Computer Science with an emphasis on programming and three years of clinical research experience as a Study Coordinator, Project Manager, Contract Research Associate or equivalent in a related field
OR High School Diploma/GED and seven years of experience
OR Associate’s Degree and five years of experience
OR Master’s Degree and two years of experience
Substantial scientific and medical knowledge across relevant therapeutic areas
Demonstrated ability to work with multiple software technologies
Knowledge of FDA regulations, GCPs and internal SOPs
Knowledge of the Code of Federal Regulations, ICH and GCP guidelines and their applications to clinical research trials
Background/ability or working with clinical studies and clinical research team members at all levels
Within 90 days of hire, must successfully complete training in Human Subjects Research (HSR) as required by the Responsible Conduct of Research guidelines adopted by the Cleveland Clinic
Preferred qualifications for the ideal future caregiver include:
Society of Clinical Research Associates (SOCRA) or Association of Clinical Research Professionals (ACRP) Certification
Grant submission and post-award experience
Physical Requirements:
Requires full range of motion, manual and finger dexterity and eye-hand coordination.
Requires standing and walking for extensive periods of time.
Requires normal or corrected hearing and vision to normal range.
Personal Protective Equipment:
Follows standard precautions using personal protective equipment as required.
Pay Range
Minimum Annual Salary: $63,250.00
Maximum Annual Salary: $96,467.50
The pay range displayed on this job posting reflects the anticipated range for new hires. A successful candidate’s actual compensation will be determined after taking factors into consideration such as the candidate’s work history, experience, skill set and education. The pay range displayed does not include any applicable pay practices (e.g., shift differentials, overtime, etc.). The pay range does not include the value of Cleveland Clinic’s benefits package (e.g., healthcare, dental and vision benefits, retirement savings account contributions, etc.).
Oversees the administrative functions of single and/or multi-institutional research trials. Coordinates/Manages daily organization and operational issues/activities related to Phase I-IV clinical research trials. Facilitates key trial communications for academic coordination, provides clinical perspective to the design and conduct of clinical trials.
Join Cleveland Clinic Research, where you will work alongside passionate caregivers and make a lasting, meaningful impact on patient care. Here, you will receive endless support and appreciation while building a rewarding career with one of the most respected healthcare organizations in the world.
Groundbreaking discoveries happen every day at Cleveland Clinic. As a Clinical Research Project Manager, you will interact with various research teams and play a crucial role in managing the clinical research that allows Cleveland Clinic to continue to innovate and drive better outcomes for patients. Clinical research is the only way that medicine comes on the market, pushing the edge of moving medicine forward. Come join a culture devoted to pushing the needle forward in healthcare.
In Pediatric Hematology and Oncology you will support research and clinical trials for our youngest cancer patients. Learn more here
A caregiver in this role works days from 8:30am-5:00pm. Start/end times may vary.
A caregiver who excels in this role will:
Oversee the administrative functions of single and/or multi-institutional research trials.
Coordinate/manage daily organization and operational issues/activities related to Phase I-IV clinical research trials.
Facilitate key trial communications for academic coordination.
Provide clinical perspective to the design and conduct of clinical trials.
Manage and coordinate a clinical trials team (external industry team members, statisticians, database programmers and researchers) responsible for data accumulation, input and analysis.
Interact with the Finance and Legal Departments to facilitate clinical trial budget, site budget and contract execution.
Maintain professional relationships with sponsors, including frequent, open communication and associated documentation.
Coordinate development, preparation, review and approval of research protocols, case report forms and regulatory documents for the conduct of research required by Institutional Review Board (IRB), Sponsor and FDA.
Collect and review regulatory documents from sites.
Communicate with institutional and central IRBs, FDA and other parties regarding protocol subject and safety issues.
Organize, coordinate, attend and participate in Investigator Meetings and training programs.
Develop and maintain planned communication with sites (i.e., newsletters, study progress updates, telephone communication, supportive reinforcement of Sponsor communication, etc.).
Analyze site strengths and weaknesses related to intended protocol and selection of qualified investigators and sites.
Assess investigator and site performance.
Lead initiatives to improve quality and make recommendations to discontinue sites if necessary.
Assist with the development, implementation and evaluation of research subject recruitment strategies, including marketing strategies, to maximize enrollment and retention.
Complete training in Human Subjects Research (HSR) as required by the Responsible Conduct of Research guidelines adopted by the Cleveland Clinic.
Perform other duties as assigned.
Minimum qualifications for the ideal future caregiver include:
Bachelor’s Degree in Nursing, Science, Healthcare or Computer Science with an emphasis on programming and three years of clinical research experience as a Study Coordinator, Project Manager, Contract Research Associate or equivalent in a related field
OR High School Diploma/GED and seven years of experience
OR Associate’s Degree and five years of experience
OR Master’s Degree and two years of experience
Substantial scientific and medical knowledge across relevant therapeutic areas
Demonstrated ability to work with multiple software technologies
Knowledge of FDA regulations, GCPs and internal SOPs
Knowledge of the Code of Federal Regulations, ICH and GCP guidelines and their applications to clinical research trials
Background/ability or working with clinical studies and clinical research team members at all levels
Within 90 days of hire, must successfully complete training in Human Subjects Research (HSR) as required by the Responsible Conduct of Research guidelines adopted by the Cleveland Clinic
Preferred qualifications for the ideal future caregiver include:
Society of Clinical Research Associates (SOCRA) or Association of Clinical Research Professionals (ACRP) Certification
Grant submission and post-award experience
Physical Requirements:
Requires full range of motion, manual and finger dexterity and eye-hand coordination.
Requires standing and walking for extensive periods of time.
Requires normal or corrected hearing and vision to normal range.
Personal Protective Equipment:
Follows standard precautions using personal protective equipment as required.
Pay Range
Minimum Annual Salary: $63,250.00
Maximum Annual Salary: $96,467.50
The pay range displayed on this job posting reflects the anticipated range for new hires. A successful candidate’s actual compensation will be determined after taking factors into consideration such as the candidate’s work history, experience, skill set and education. The pay range displayed does not include any applicable pay practices (e.g., shift differentials, overtime, etc.). The pay range does not include the value of Cleveland Clinic’s benefits package (e.g., healthcare, dental and vision benefits, retirement savings account contributions, etc.).
See All 9 Clinical Project Manager Jobs in Ohio
Find roles in Ohio that match your experience and apply in just a few clicks.
Find Clinical Project Manager JobsClinical Project Manager Jobs by City in Ohio
Where Ohio roles are concentrated, by current openings.
Clinical Project 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 project manager jobs across Ohio.
- Bachelor's degree in life sciences, nursing, pharmacy, or a related clinical field required
- PMP or CAPM certification strongly preferred by Ohio research and health system employers
- Minimum two to five years of clinical trial or research operations experience expected
- Demonstrated knowledge of ICH-GCP guidelines and FDA regulatory submission processes required
- Experience managing CRO relationships, site budgets, and study timelines across multiple sites
- Proficiency with clinical trial management systems such as Medidata Rave or Veeva Vault
Clinical Project Manager Jobs in Ohio: Frequently Asked Questions
How do you become a clinical project manager in Ohio?
Most clinical project managers in Ohio start with a bachelor's degree in a life sciences, nursing, or health-related field, then build experience in clinical research coordination or monitoring roles before moving into project management. Ohio does not require a state-issued license specific to this role, but earning a Project Management Professional certification or a Clinical Research Associate credential through ACRP or SOCRA strengthens hiring prospects considerably with major Ohio health systems and CROs.
How much do clinical project managers make in Ohio?
Clinical project managers in Ohio earn a median of about $95,770 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $59,280 for the lowest 10% to over $160,570 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire clinical project managers in Ohio?
Employers hiring clinical project managers in Ohio right now include Medpace, OhioHealth, and UC Health, based on current listings on Migrate Mate as of September 2026. Ohio's concentration of large integrated health systems, pharmaceutical headquarters, and contract research organizations means steady, year-round demand rather than seasonal spikes.
Which Ohio cities have the most clinical project manager jobs?
Cincinnati, Columbus, and Ohio account for the largest share of clinical project manager openings in Ohio. Columbus leads because of its dense cluster of health system headquarters, Cardinal Health's corporate base, and a growing biotech corridor, while Cleveland's strength comes from the Cleveland Clinic and University Hospitals research enterprises, and Cincinnati benefits from proximity to major pharmaceutical and CRO operations on both sides of the state line.
Are there remote clinical project manager jobs in Ohio?
Yes, and more than most clinical roles allow. About 17% of clinical project manager openings tied to Ohio are remote or hybrid as of September 2026, reflecting how much of the role involves data review, vendor oversight, and cross-functional coordination rather than hands-on site work. Sponsor-side and CRO project management positions tend to offer the most remote flexibility, while site-facing roles and those requiring regular investigator interaction are more likely to require an Ohio presence.
How can I get hired as a clinical project manager in Ohio with little or no experience?
The most realistic entry path is starting as a clinical research coordinator at a large Ohio academic medical center, where institutions like the Ohio State University Wexner Medical Center and University Hospitals actively hire coordinators without prior research experience and provide structured training. From there, coordinators build the protocol management and site relationship skills that transfer directly into a junior project manager role. Earning an entry-level ACRP certification while coordinating strengthens a candidacy, and internal postings at Ohio-based CROs often give coordinators a first step into project oversight without requiring a formal PM background.
Where can I find and apply to clinical project manager jobs in Ohio?
You can find and apply to clinical project manager jobs in Ohio on Migrate Mate, which lists current Ohio openings updated regularly. Search the listings, find roles that match your experience and preferred location or remote arrangement, and apply directly to the ones that fit.
See All 9 Clinical Project Manager Jobs in Ohio
Find roles in Ohio that match your experience and apply in just a few clicks.
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