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Medical Device Clinical Jobs in Ohio (NOW HIRING)

Cleveland Diagnostics Inc.

Clinical Study Manager

Cleveland, OH · On-site

$90K - $120K/yr

  • Dental

  • Vision

  • Retirement

  • PTO

Experience in IVD or medical device clinical research strongly preferred. * Clinical research certification (e.g. ACRP, SOCRA) strongly preferred. * Knowledge of Good Clinical Practice (GCP)/ICH and ...

Cleveland Diagnostics, Inc.

Clinical Study Manager

Cleveland, OH · On-site

$90K - $120K/yr

  • Dental

  • Vision

  • Retirement

  • PTO

Experience in IVD or medical device clinical research strongly preferred. * Clinical research certification (e.g. ACRP, SOCRA) strongly preferred. * Knowledge of Good Clinical Practice (GCP)/ICH and ...

Medpace

Medical Imaging Analyst

Cincinnati, OH · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Perform quality assurance checks on medical imaging data collected during medical and device clinical trials to ensure protocol specific requirements are met; * Perform established image processing ...

Medpace, Inc.

Medical Imaging Analyst

Cincinnati, OH · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Perform quality assurance checks on medical imaging data collected during medical and device clinical trials to ensure protocol specific requirements are met; * Perform established image processing ...

Medpace, Inc.

Medical Imaging Analyst

Cincinnati, OH · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Perform quality assurance checks on medical imaging data collected during medical and device clinical trials to ensure protocol specific requirements are met; * Perform established image processing ...

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All JobsMedical Device Clinical JobsMedical Device Clinical Jobs in Ohio

Medical Device Clinical information

See Ohio salary details

$94.6K

$107K

$117.9K

How much do medical device clinical jobs pay per year?

As of Aug 18, 2026, the average yearly pay for medical device clinical in Ohio is $106,953.00, according to ZipRecruiter salary data. Most workers in this role earn between $100,800.00 and $113,100.00 per year, depending on experience, location, and employer.

What is a medical device clinical professional?

Medical Device Clinical professionals are specialists who oversee and manage the clinical aspects of medical device development and testing. They are responsible for planning, executing, and monitoring clinical trials to ensure medical devices are safe and effective for patient use. Their work involves collaborating with regulatory bodies, healthcare providers, and research organizations to collect and analyze clinical data. These professionals play a key role in ensuring that medical devices comply with regulatory requirements before they reach the market.

What are the key skills and qualifications needed to thrive as a medical device clinical specialist?

To thrive as a Medical Device Clinical Specialist, you need a solid background in life sciences or nursing, strong clinical knowledge, and often a relevant degree or certification. Familiarity with medical device technologies, regulatory standards, and clinical trial management systems is typically required. Excellent communication, problem-solving, and relationship-building skills help you effectively train healthcare professionals and support product adoption. These skills are crucial for ensuring safe, effective device use and successful integration into clinical environments.

What are some common challenges faced by professionals in medical device clinical roles, and how can they be addressed?

Professionals in Medical Device Clinical roles often encounter challenges such as navigating complex regulatory requirements, coordinating multi-site clinical trials, and ensuring timely patient recruitment. To address these, strong organizational skills, clear communication with cross-functional teams, and ongoing education about evolving regulations are essential. Building strong relationships with investigators and site staff can also help streamline trial processes and ensure high-quality data collection.

What is the difference between Medical Device Clinical vs Medical Device Quality Assurance?

AspectMedical Device ClinicalMedical Device Quality Assurance
CertificationsClinical Research Certification, GCP trainingISO 13485, GMP training
Work EnvironmentHospitals, clinics, clinical research settingsManufacturing facilities, quality labs
Employer & Industry UsageMedical device companies, research organizationsManufacturers, regulatory agencies
Primary FocusClinical trials, patient safety, device efficacyProduct quality, compliance, process validation

Medical Device Clinical roles focus on conducting clinical trials and ensuring device safety and efficacy, often working directly with patients. In contrast, Medical Device Quality Assurance emphasizes maintaining product quality, regulatory compliance, and manufacturing standards. Both roles are essential in the medical device industry but serve different functions within the product lifecycle.

What does a medical device clinical specialist do?

A medical device clinical specialist is responsible for training healthcare professionals on the proper use of medical devices, providing technical support, and ensuring compliance with regulatory standards. They often work closely with sales teams, conduct product demonstrations, and gather user feedback to improve device performance and safety.

What cities in Ohio are hiring for Medical Device Clinical jobs?

Cities in Ohio with the most Medical Device Clinical job openings:

Medical Device Clinical jobs near you
Infographic showing various Medical Device Clinical job openings in Ohio as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 12% Part Time, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $106,953 per year, or $51.4 per hour.

Clinical Study Manager

Cleveland Diagnostics Inc.

Cleveland, OH • On-site

$90K - $120K/yr

Full-time

Dental, Vision, Retirement, PTO

Re-posted 24 days ago

Job description

Our team is growing, and we currently have an immediate opening for a Clinical Study Manager
Title: Clinical Study Manager
Location: Onsite (Cleveland, Ohio)
Reports to: Director, Clinical Operations
Job Description: This position will oversee assigned clinical research projects, protocol development, site management, monitoring, TMF management, cross-departmental collaboration and communication, and documenting and tracking execution of projects to adhere to milestones, budgets, and targeted timelines.
Essential Duties and Responsibilities
  • Manage end-to-end lifecycle of assigned IVD clinical research projects, including startup, site management, monitoring, and closeout. Coordinate IRB submissions, laboratory shipments and incoming samples, sample receipt logging, kit creation and inventory, and ensure study deliverables are achieved on time and within budget.
  • Oversee TMF, CTMS, and database for assigned projects. Participate in development of protocols, ICFs, CRFs, and other study-related documents. Build study budgets and timelines, establish milestones, and coordinate site selection and activation. Track metrics and summarize clinical data for project updates, reports and publications.
  • Serve as the primary liaison between the sponsor, vendor, sites, and internal cross-functional teams for assigned projects.
  • Ensure project compliance with ICH-GCP guidelines, IRB requirements, FDA regulations, and any other applicable requirements.
  • Contribute to the forecasting and management of resources. Identify future potential studies to address unmet needs.
  • Support the onboarding of new technologies, progression of scientific innovation projects, and process improvement initiatives.
  • Perform all other duties as assigned.
Qualifications/Requirements
  • Bachelor's degree in a health or science field required.
  • At least 5 years of experience in clinical research, with specific experience in studies used for FDA/regulatory submission required. Direct trial management experience and prior experience working at the sponsor/CRO level required.
  • Experience in IVD or medical device clinical research strongly preferred.
  • Clinical research certification (e.g. ACRP, SOCRA) strongly preferred.
  • Knowledge of Good Clinical Practice (GCP)/ICH and medical device clinical trial guidelines, rules, and regulations. Understanding of Good Laboratory Practice (GLP), research safety, HIPAA, confidentiality, and regulatory standards amp; requirements.
  • Strong organizational skills and attention to detail. Ability to work autonomously and strong decision-making skills.
  • Excellent written and verbal communication skills.
  • Ability to travel overnight and out-of-state occasionally (20%)
Physical Requirements/ Working Conditions/Equipment Used:
  • Office reachable by elevator but should be able to climb stairs if needed
  • Light lifting may be required (up to 25 pounds)
  • Ability to work in an environment with exposure to hazardous chemicals and biohazards
  • Ability to operate a computer throughout course of day
  • General office and HVAC noise amp; fluorescent and/or LED lighting
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Cleveland Diagnostics, Inc., is developing highly efficacious, lab-friendly, affordable diagnostics tests using proprietary technology to improve cancer diagnostics. We pride ourselves in fostering a family-focused, friendly, and flexible organization that places our employee’s well-being and happiness as the primary reason for our success. Are you interested in building your career with a team of industry professionals while making a lasting impact to the lives of millions of people? Bring your talents to Cleveland Diagnostics.
Cleveland Diagnostics offers an extremely robust benefits package which includes:
  • 100% Employer-paid medical for single coverage effective on your date of hire and 50% employer-paid medical for spouse/dependent coverage
  • 100% Employer-paid Dental amp; Vision for entire family
  • No cost for employee coverage for Group Term Life, Short- amp; Long-Term Disability
  • 4% retirement contribution Employer match
  • Incentive Performance Plan amp; Stock Option Program amp; Commission (Sales Account Execs)
  • Paid Family Leave Program
  • Generous PTO plan amp; holiday program
  • Flexible work schedule amp; lucrative employee referral program
  • Salary range may vary by work state/geographical region/territory
  • Easy to get to office location with newly built-out office space
  • Free coffee, snacks and other goodies all day long
Cleveland Diagnostics is an equal opportunity employer and is committed to providing a workplace free from harassment and discrimination. We celebrate the unique differences of our employees because that is what drives curiosity, innovation, and the success of our business. EEO is the Law. Applicants can learn more about the company’s status as an equal opportunity employer by viewing the federal EEO is the Law poster on our careers page. Accommodations are available for applicants with disabilities.

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