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Clinical Research Operations Jobs in Ohio (NOW HIRING)

TriHealth

Clinical Research Site Manager

Montgomery, OH · On-site

$85 - $120/hr

The Clinical Research Site Manager plays a pivotal role at the intersection of patient care ... Drive strategic and operational excellence - Lead protocol evaluation, process improvement, and ...

panoramic

Clinical Research Coordinator II

Cincinnati, OH

$23.25 - $31/hr

... operations at the site level. In this role, you'll work alongside nephrology physicians and research professionals to bring innovative therapies to patients with chronic kidney disease and related ...

MD Ally

Senior Clinical Research Coordinator

Dayton, OH · On-site

$80 - $110/hr

As a Senior Clinical Research Coordinator (Sr. CRC) at Iterative Health you will serve as a key ... Assess operational challenges, identify solutions, and recommend process improvements to enhance ...

New

Ohio Health

Research Assistant

Upper Arlington, OH

$17.50 - $24/hr

The purpose of this position is to provide coordination and support for OHRI Research Operations as it relates to therapeutic/interventional clinical trials, academic research, regulatory, quality ...

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All JobsClinical Research Operations JobsClinical Research Operations Jobs in Ohio

Clinical Research Operations information

See Ohio salary details

$46.6K

$102K

$179.7K

How much do clinical research operations jobs pay per year?

As of Aug 20, 2026, the average yearly pay for clinical research operations in Ohio is $102,044.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,000.00 and $116,500.00 per year, depending on experience, location, and employer.

What is clinical research operations?

Clinical research operations refer to the planning, execution, and management of clinical trials and studies that test new medical treatments, drugs, or devices. This field ensures that studies are conducted ethically, efficiently, and in compliance with regulatory guidelines. Professionals in clinical research operations coordinate activities such as patient recruitment, data collection, regulatory submissions, and quality control. Their work is essential for advancing medical knowledge and ensuring the safety and effectiveness of new healthcare interventions.

What are the key skills and qualifications needed to thrive in clinical research operations?

To thrive in Clinical Research Operations, you need a strong understanding of clinical trial protocols, regulatory guidelines (such as ICH-GCP), and project management, 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 often required. Exceptional organizational skills, attention to detail, and effective communication are crucial soft skills for coordinating teams and ensuring compliance. These competencies are vital for maintaining data integrity, meeting regulatory standards, and successfully managing complex clinical studies.

What are some common challenges faced in clinical research operations and how can they be addressed?

Professionals in clinical research operations often encounter challenges such as managing complex regulatory requirements, coordinating across multidisciplinary teams, and ensuring adherence to strict timelines. Successfully addressing these challenges typically involves strong project management skills, effective communication with stakeholders, and staying updated on regulatory changes. Leveraging technology for data management and fostering a collaborative work environment can also help streamline processes and improve trial outcomes.

What is the difference between Clinical Research Operations vs Clinical Research Coordinators?

AspectClinical Research OperationsClinical Research Coordinators
CredentialsTypically requires a degree in life sciences, certifications like CCRP or RACOften requires a bachelor's degree in health sciences or related field, with certifications like CCRP beneficial
Work EnvironmentOversees multiple studies, manages teams, and collaborates with sponsors and regulatory bodiesWorks directly with study participants, manages data collection, and ensures protocol adherence
Employer & Industry UsageUsed in pharmaceutical companies, CROs, and research institutionsCommonly employed in hospitals, clinics, and research sites

Clinical Research Operations professionals focus on managing entire research programs, budgets, and teams, while Clinical Research Coordinators handle day-to-day study activities and participant interactions. Both roles are essential but differ in scope and responsibilities within the clinical research field.

Is clinical research operations a good career?

Clinical research operations involves managing and coordinating clinical trials to ensure they meet regulatory standards and are completed efficiently. It offers opportunities for growth, requires strong organizational and communication skills, and often involves working with cross-functional teams and specialized software. Many professionals find it a rewarding field with stable employment prospects in the healthcare and pharmaceutical industries.

What are the most commonly searched types of Clinical Research Operations jobs in Ohio?

The most popular types of Clinical Research Operations jobs in Ohio are:

What are popular job titles related to Clinical Research Operations jobs in Ohio?

For Clinical Research Operations jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Clinical Research Operations jobs in Ohio look for?

The top searched job categories for Clinical Research Operations jobs in Ohio are:

Clinical Research Operations jobs near you
Infographic showing various Clinical Research Operations job openings in Ohio as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 9% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $102,044 per year, or $49.1 per hour.

Clinical Research Business Operations Specialist, Peds Hematology/Oncology

Jobtailor

Cleveland, OH • On-site

$70 - $100/hr

Other

Posted 2 days ago

New

Job description

Responsibilities
  • Track, manage, and report finances and accounting related to clinical research services and tasks performed by team. (40%)
  • Develop and monitor programs related to quality assurance and business projection (20%).
  • Assist Manager in developing budgets for studies and research services. (20%)
  • Track, manage, and report milestones and metrics related to research operations. (10%)
  • Responsible for ensuring compliance with monthly, quarterly and annual reporting guidelines to internal and external regulatory agencies (including CRC, NIH, FDA, CTSC, etc.) (5%)
  • Assist Manager in managing multiple committees and initiatives to further grow and develop research services. (5%)
  • Additional Responsibilities: Performs other duties as assigned. Complies with all policies and standards.
Requirements
  • Associate's Degree in business with at least 6 years in clinical research business operations (Required) or Bachelor's Degree in business with at least 4 years experience in clinical research business operations (Required)
  • 4+ years business operations experience with demonstrated ability to prioritize and manage the execution of multi-discipline team projects. (Required)
  • Clinical research operations experience (Preferred)
  • Business analyst experience (Preferred)
  • Supervisory or Project Management experience (Preferred)
  • Detail-oriented, results-driven person with the ability to manage successful completion of project milestones against pre-determined timelines for multiple projects concurrently. (Required proficiency)
  • Analytical and problem-solving skills needed to evaluate and report key metrics and other operational information. (Required proficiency)
  • Documented experience with process improvement assessment. (Required proficiency)
  • Able to function with minimal supervision. (Required proficiency)
  • Ability to work in a multidisciplinary, collaborative, team environment. (Required proficiency)
  • Excellent verbal, written and communication skills to be able to develop and maintain effective communication strategies and work collaboratively within a multidisciplinary team environment. (Required proficiency)
  • Strong computer skills to automate processes and provide reports as needed - Excel, Word, PowerPoint, database queries). (Required proficiency)
Core Competencies

Demonstrates expertise in clinical research business operations, including financial management, quality assurance, and compliance with regulatory guidelines. Proficient in project management and process improvement, with strong analytical skills to evaluate and report on key metrics.

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