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Study Com Jobs in Ohio (NOW HIRING)

Impact.com

Product Marketing Manager II

Columbus, OH

$110K - $130K/yr

About impact.com impact.com is the world's leading commerce partnership marketing platform ... Strong research and analytical skills -- comfortable designing and running VoC studies ...

Impact.com

Product Marketing Manager II

Columbus, OH · On-site

$110K - $130K/yr

About impact.com impact.com is the world's leading commerce partnership marketing platform ... Strong research and analytical skills - comfortable designing and running VoC studies, interpreting ...

Cart.com

Maintenance Technician I

Groveport, OH · On-site

Who we are: * We're Cart.com, one of the fastest growing commerce enablement companies in the world ... study and is willing to complete the remainder within 2 years from date of hire. Physical Work ...

Cart.com

Maintenance Technician I

Groveport, OH · On-site

Who we are: * We're Cart.com, one of the fastest growing commerce enablement companies in the world ... study and is willing to complete the remainder within 2 years from date of hire. Physical Work ...

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Showing results 1-20

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 Jun 12, 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.

How much does Study.com pay?

Study.com offers various roles such as content creators and educators, with pay rates typically ranging from $15 to $30 per hour depending on the position and experience. Compensation may also include bonuses or incentives based on performance and project requirements.

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 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 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.

How to make $10,000 a month with no degree?

Study Com roles such as online tutoring, freelance writing, or digital marketing can generate high income without a degree by leveraging skills, building a strong portfolio, and using platforms like Upwork or Fiverr. Success depends on experience, reputation, and consistent effort to scale income over time.

Is study.com legit to work for?

Study.com offers various remote teaching and content creation positions, and many employees report it as a legitimate employer. However, as with any job opportunity, it is advisable to research current reviews and verify the specific role's requirements before applying.

What are Study Com jobs?

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.

How can I make 2000 a week working from home?

Study Com and similar remote roles often pay based on the number of completed tasks or hours worked, with earnings varying by workload and efficiency. To make $2000 a week, you typically need to work full-time hours consistently, develop strong study or communication skills, and possibly hold relevant certifications or experience to increase earning potential.
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 June 2026, with employment types broken down into 2% As Needed, 82% Full Time, 11% Part Time, 2% Temporary, 2% Contract, and 1% Nights. Highlights an 94% Physical, 3% Hybrid, and 3% Remote job distribution, with an average salary of $119,113 per year, or $57.3 per hour.
Clinical Research Study Assistant

Clinical Research Study Assistant

Optima Dermatology

Boardman, OH • On-site

Full-time

Posted 18 days ago

Job description

Multi-site Dermatology Group Seeks Medical Receptionist / Clinical Research Study Assistant
Optima Dermatology is recruiting an experienced full time Medical Receptionist / Clinical Research Study Assistant to join our growing Dermatology and Medical Aesthetics group in Boardman, OH.
Position Summary
The Medical Receptionist (MR)/Clinical Research Study Assistant (CRSA) is responsible for a variety of activities in support of clinical research studies. The MR-CRSA works closely with and carries out the directives of the Sub-Investigator in all aspects of the care and treatment of clinical research subjects in compliance with study protocols throughout the research study. The MR-CRSA is responsible for his/her delegated tasks as it relates to but is not limited to, the following areas: protocol requirements, patient visits (paper and electronic); laboratory and test article. The MR-CRSA must have knowledge of protocol design and Good Clinical Practices (GCP) as set forth by the Federal Regulations and International Conference of Harmonization (ICH) Guidelines for protecting human subjects and conducting clinical research. Knowledge of the International Air Transport Association (IATA) regulations for the transportation of Dangerous Goods is also necessary. Under the direction of the Sub-Investigator, the MR-CRSA will help ensure protocol compliance, Investigational Article accountability, and proper follow-up during the clinical trial.
TYPICAL PHYSICAL DEMANDS: Physically capable of lifting, moving, or transporting supplies, medical records, and equipment within reasonable weight limits. Physically capable of reading and reviewing handwritten chart notations. Physically capable of bending, sitting, or standing for extended periods of time, reaching, and climbing to retrieve or store medical records. Physically capable of manually entering data into an electronic database using a keyboard. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.
TYPICAL WORK CONDITIONS: Fast-paced clinical research center environment. Must be able to adjust and adapt to changing conditions.
QUALIFICATIONS, REQUIREMENTS, and EDUCATION: Minimum: High School Diploma. Preferred: Associate degree in a medical-related field and one-year clinical research experience.
ESSENTIAL SKILLS:
  • Maintain the highest level of professional conduct in the presence of investigators, subjects, research staff, sponsors, etc.
  • Able to perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study-specific protocols
  • Computer skills with the capability of using clinical trial databases, electronic data capture, Microsoft Word Office
  • Ability to communicate clearly using excellent verbal and written communications skills
  • Possess exceptional organizational and prioritization skills as demonstrated by planning objectives and strategies to ensure that the process/requirements for the flow of clinical research information are optimized, such as charting is completed accurately and thoroughly and ready for EDC processing within 48 hours of the patient visit.
  • Ability to problem-solve, prioritize quickly and accurately, and multi-task to facilitate workflow
  • Ability to work independently in a fast-paced environment, as well as work collaboratively as a team
  • Possess and utilize excellent interpersonal skills with patients, staff, and others
  • Meticulous and detail-oriented
  • Ability to perform Phlebotomy, Urinary Pregnancy Test
  • Ensure the proper collection, processing, and shipment of biospecimens (e.g., centrifuge, freezing, refrigeration.

DUTIES AND RESPONSIBILITIES:
Medical Receptionist:
  • Welcomes and receives patients/visitors to Optima Research by greeting them with a warm, pleasant affect
  • Provides study candidates and participants with appropriate forms for their visit
  • Gathers information from study candidates/participants upon arrival using the appropriate form for their visit
  • Notifies clinical staff when study candidates/participants are ready to be seen for their appointment
  • Pulls and prepares study participant binders for scheduled visits the day prior
  • In collaboration with the Clinical Research Coordinators, schedules study participant appointments within the visit window as designated by the study protocol in CRIO
  • Provides study participants with appropriate compensation at the conclusion of each study visit, obtaining participant signature for cash distribution and maintaining stipend cash log
  • Answers phones using professional telephone etiquette
  • Knowledgeable of phone system and routes calls appropriately or takes detailed messages if call recipient is unavailable, documents messages in CRIO
  • Notifies subjects of upcoming visits the day before
  • Responds to and sends faxes
  • Distributes incoming faxes to the appropriate recipient
  • Knowledgeable in using front office equipment, such as copier, computer, etc.
  • Complies with HIPPA guidelines, protecting and respecting the privacy of all patient information and records
  • Stores all files in a permanent, dry, and safe location
  • Maintains a cooperative, helpful, and pleasant affect, creating and/or contributing to an atmosphere of collaboration and team cohesiveness
  • Maintains neatness of the front office, patient reception area, and patient lounge
  • Cleans surfaces and chairs of patient reception area, patient lounge, and patient treatment rooms at the end of each business day with germicidal wipes
  • Assists clinical research coordinators and other staff as needed
  • Assists in the day-to-day operations, as needed and as assigned

Clinical Trial Process:
  • Assists in facilitating the daily clinical trial activities
  • Reviews and comprehends each protocol
  • Thoroughly and accurately completes study participant logs, keeping them current
  • Assists in screening, recruiting, enrolling, and maintaining research participants
  • Ensures adherence to protocol requirements
  • Knowledgeable of the storage/temperature requirements for all assigned study medications stored on site
  • Ensures appropriate specimen collection, processing, and shipment per study protocol
  • Communicates lab alerts to appropriate persons in a timely manner.
  • Maintains study source documents in the subject chart (e.g., medical history, laboratory reports, ECG, etc.)
  • Ensure that all daily subject visit requirements are completed prior to daily departure.
  • Administers questionnaires/diaries per protocol

Other:
  • Completes Continuing Education/In-service Education Requirements in the designated timeframe
  • Adheres to Optima Policies and Procedures, Employee Guidebook, and Standard Operating Procedures
  • Proper archiving of all documents and supplies at study close-out (i.e., breaking down study charts)
  • Assisting in maintaining IP temperature (ambient and refrigerated) and reporting any excursion that may occur

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