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Study Com Jobs in Ohio (NOW HIRING)

Pure Barre Belden

Fitness Instructor

Brecksville, OH · On-site

For more information, visit: purebarre.com Qualifications: * Enthusiastic, confident and outgoing ... Diligent planning and preparation before each class, including diligent study of choreography and ...

Pure Barre Belden

Fitness Instructor

Brecksville, OH · On-site

For more information, visit: purebarre.com Qualifications: * Enthusiastic, confident and outgoing ... Diligent planning and preparation before each class, including diligent study of choreography and ...

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Showing results 21-40

All JobsStudy Com JobsStudy Com Jobs in Ohio

Study Com information

See Ohio salary details

$20.9K

$119.1K

$195.8K

How much do study com jobs pay per year?

As of Sep 7, 2026, the average yearly pay for study com in Ohio is $119,113.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,800.00 and $149,300.00 per year, depending on experience, location, and employer.

What is a study com?

Study.com jobs refer to employment opportunities with Study.com, an online education platform that provides video lessons, study guides, and other educational resources. Job roles at Study.com can include content writers, curriculum developers, video editors, software engineers, and customer support specialists. Employees work to create and maintain high-quality educational content and ensure a positive learning experience for users. Some positions are remote or freelance, offering flexible work options. Working at Study.com can be a good fit for those passionate about education and technology.

What are the typical responsibilities of a study coordinator in a clinical research setting?

A Study Coordinator, often referred to as a Clinical Research Coordinator, is responsible for managing daily operations of clinical trials. This includes recruiting and screening study participants, obtaining informed consent, scheduling and conducting study visits, collecting and recording data, and ensuring compliance with regulatory requirements. Coordinators also act as a liaison between investigators, sponsors, and study participants, making strong organizational and communication skills essential. The role offers opportunities to learn about various aspects of clinical research, paving the way for career advancement into project management or regulatory affairs.

What are the key skills and qualifications needed to thrive as a study coordinator, and why are they important?

To thrive as a Study Coordinator, you need a solid understanding of clinical research protocols, regulatory compliance, and project management, often supported by a degree in life sciences or healthcare. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certification such as CCRC or CCRP is typically required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for coordinating between study teams, participants, and regulatory bodies. These competencies ensure studies are conducted ethically, efficiently, and in accordance with regulatory standards, which is vital for research integrity and successful trial outcomes.

What is the difference between Study Com vs Study Coordinator?

AspectStudy ComStudy Coordinator
Required CredentialsTypically a bachelor's degree, sometimes certifications in clinical researchUsually a bachelor's degree, often with certifications like CCRP or CCRC
Work EnvironmentOffice-based, research institutions, hospitalsClinical settings, hospitals, research sites
Employer & Industry UsageResearch organizations, pharmaceutical companies, academic institutionsHospitals, clinics, research sites
Common Search & ComparisonOften compared for roles in clinical research teamsFrequently compared with Study Com as a supporting role

Study Coordinators and Study Com roles both support clinical research but differ mainly in scope and responsibilities. Study Coordinators typically handle day-to-day trial management, patient coordination, and data collection, while Study Com may focus on broader communication and administrative tasks within research projects. Both roles require relevant certifications and work in similar environments, making them closely related in the clinical research industry.

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

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

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

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

What cities in Ohio are hiring for Study Com jobs?

Cities in Ohio with the most Study Com job openings:

Study Com jobs near you
Infographic showing various Study Com job openings in Ohio as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 17% Part Time, 1% Temporary, and 5% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $119,113 per year, or $57.3 per hour.

Clinical Research Coordinator (level dependent on experience)

CTI

Cincinnati, OH • On-site, Remote

$23.25 - $31/hr

Full-time

Medical, Life, PTO

Posted 18 days ago

Job description

Coordinate the conduct of Phase I through Phase IV clinical research studies in accordance with Good Clinical Practices (GCPs), International Harmonization Guideline and Standard Operating Procedures (SOPs) beginning with pre-study planning through successful completion of all study visits.  

What You'll Do: 

  • Maintain a good level of knowledge and understanding of assigned protocols, including all protocol requirements for study visits, obtaining informed consent, study visit schedules, tests, procedures, laboratory information, and drug accountability requirements 
  • Recruit subject volunteers for studies; Work with the Recruitment Department with developing  study-related materials and interview questionnaires 
  • Create source templates for study documentation, complete case report forms, and other study specific documents seeking assistance from Senior Clinical Research Coordinator, Principal Clinical Research Coordinator, Team Leader or Clinical Site Director, as needed 
  • Ensure consistency and effective communication during study visits and assure all procedures are conducted in compliance with the clinical protocol; Maintain subject safety, assess feedback from study participant and refer to investigators or other professionals as needed; If applicable, administer study medications based on state licensure, account for medications used 
  • Coordinate and conduct study visits; Assure all procedures are conducted in compliance with the clinical protocol and in accordance with all applicable regulations and in compliance with GCPs 
  • Interact with Investigators or study sponsors as needed to assure the study participant receives appropriate medical evaluation and care when needed 
  • Interact with the sponsor Clinical Research Associate to facilitate the sponsor monitoring and database clean-up process 
  • Attend sponsor Investigator/Study Coordinator meetings as needed for assigned protocols 
  • Conduct clinical research in compliance with all applicable regulations; Request assistance and technical advice from Senior Clinical Research Coordinator, Principal Clinical Research Coordinator, Team Leader, or Clinical Site Director, as needed 
  • Actively seeks out development opportunities 
  • Behave cooperatively and constructively; Follow all company policies, state, local, federal, and other applicable laws and guidelines; Comply with all job-specific requirements 

What You'll Bring: 

  • 1+ year of experience as a clinical research coordinator or in a similar position within the medical or mental health field 
  • Bachelor’s degree in life sciences or equivalent combination of related experience and education in the medical or mental health field
  • Clinical Research Coordinator Certification (CCRC) is preferred 
  • Associate or Bachelor’s Degree in Nursing is preferred
  • Advanced Cardiac Life Support (ACLS) is preferred 
       
         

        Why CTI? 

        • Advance Your Career – We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through tuition reimbursement and a dedicated training department.
        • Join an Award-Winning and Valued Team – We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. We support a work-life balance and the importance of time with family by offering generous health benefits and vacation packages, hybrid work from home opportunities, and paid parental leave. We also encourage care for the world around us through our unique CTI Cares program.
        • Make a Lasting Impact – We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market.

        Important Note
        In light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of our team will reach out to you directly from an @ctifacts.com email address to guide you through our interview process. Please ensure you are applying for jobs directly on our website (www.ctifacts.com) or from our verified LinkedIn page.
        Please Note 

        • We will never communicate directly with you via Microsoft Teams Messaging or by text message
        • We will never ask for your bank account information at any point during the recruitment process

        Equal Opportunity Employer/Veterans/Disabled

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