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Study Monitor Jobs in Ohio (NOW HIRING)

Cleveland Diagnostics, Inc.

Clinical Study Manager

Cleveland, OH · On-site

$90K - $120K/yr

  • Dental

  • Vision

  • Retirement

  • PTO

... management, monitoring, TMF management, cross-departmental collaboration and communication, and ... Build study budgets and timelines, establish milestones, and coordinate site selection and ...

NAMSA

Associate Study Director

Northwood, OH · On-site

Assists in the coordination of study conduct tasks from study initiation to study completion ... monitors. The Associate must occasionally lift and/or move up to 50 pounds. Specific vision ...

Beacon Biosignals

Sleep Study Support Specialist

Cleveland, OH · On-site +1

$17.50 - $23.50/hr

  • PTO

Monitor and complete test scheduling and monitor return calls to ensure patients receive timely support. * Schedule and coordinate patient testing while ensuring appointments and study information ...

Cleveland Clinic

Registered Monitor Technician

Cleveland, OH · On-site

$25.13 - $38.33/hr

  • Medical

  • Dental

  • Vision

  • Retirement

A Registered Monitor Technician monitors electrophysiological data on patients in special recording ... Assists physicians in research studies, protocols and documentation. Minimum qualifications for the ...

Imh

Lutheran Sleep Tech CPSGT/RPSGT/RRT

Cleveland, OH · On-site

$26.74 - $41.28/hr

Monitors and documents on patients undergoing physiologic sleep studies. * Monitors and tracks equipment and supplies. * Completes record keeping and charting. * Ability to address and solve both ...

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Showing results 21-40

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Study Monitor information

What is a study monitor?

A Study Monitor, also known as a Clinical Research Associate (CRA), is responsible for overseeing clinical trials to ensure they comply with regulatory guidelines, study protocols, and ethical standards. They monitor site activities, review data accuracy, and ensure participant safety. Study Monitors work closely with investigators, site staff, and sponsors to ensure the integrity of trial results and adherence to Good Clinical Practice (GCP) guidelines.

What are the key skills and qualifications needed to thrive as a study monitor?

To thrive as a Study Monitor, you need a strong understanding of clinical trial protocols, regulatory guidelines (such as GCP), and data integrity principles, typically supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are commonly expected. Excellent attention to detail, strong organizational skills, and effective communication are crucial soft skills. These competencies ensure high-quality study oversight, compliance with regulations, and smooth collaboration among clinical research teams.

What are some common challenges study monitors face during clinical trials?

Study Monitors often encounter challenges such as ensuring consistent protocol adherence across multiple sites, managing discrepancies in data, and navigating tight timelines for site visits and reporting. They must adapt quickly to evolving regulatory requirements and effectively communicate any issues or deviations to investigators and sponsors. Being proactive in identifying potential risks and fostering strong relationships with site staff can help minimize these challenges. As a result, successful Study Monitors need to be resourceful, detail-oriented, and skilled at balancing regulatory compliance with practical problem-solving in dynamic trial environments.

How do you become a study monitor?

To become a study monitor, candidates typically need to be students with good academic standing and demonstrate responsibility. The process often involves applying through the school or organization, sometimes including an interview or recommendation, and may require training on supervision and safety protocols.

What are popular job titles related to Study Monitor jobs in Ohio?

For Study Monitor jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Study Monitor jobs in Ohio look for?

The top searched job categories for Study Monitor jobs in Ohio are:

Study Monitor jobs near you
Infographic showing various Study Monitor job openings in Ohio as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 10% Part Time, 3% Contract, and 1% Nights. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution.

Clinical Study Manager

Cleveland Diagnostics Inc.

Cleveland, OH

$90K - $120K/yr

Full-time

Dental, Vision, Retirement, PTO

Re-posted 25 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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