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Research Coordinator Jobs in Columbus, OH (NOW HIRING)

Centricity Research

Clinical Research Coordinator

Columbus, OH · On-site

$23.50 - $31.25/hr

About the role We are seeking a Clinical Research Coordinator I (CRC I) to join our research team. In this role, you will support the successful execution of clinical studies by performing a mix of ...

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How much do research coordinator jobs pay per year?

As of May 27, 2026, the average yearly pay for research coordinator in Columbus, OH is $77,822.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,900.00 and $96,100.00 per year, depending on experience, location, and employer.

What Is a Research Coordinator?

A research coordinator supervises the daily activities of a study and monitors the activities of the subjects and researchers. As a research coordinator, your duties revolve around making sure that the study is conducted ethically and does not violate the research guidelines of the governing board or other agency. In short, you are responsible for making sure the study has as few flaws in its methodology as possible. You are also in charge of most administrative tasks. In this role, you can work on medical, technological, psychological, or other types of research projects, but you may work on clinical research most often.

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

To thrive as a Research Coordinator, you need strong organizational abilities, attention to detail, and a relevant bachelor's degree or higher in a scientific or health-related field. Familiarity with research compliance systems, data management tools, and Institutional Review Board (IRB) protocols is commonly required. Excellent communication, problem-solving, and multitasking skills help you manage studies and collaborate effectively with diverse teams. These skills ensure the smooth execution of research projects, regulatory compliance, and the reliability of study outcomes.

What are some common challenges Research Coordinators face when managing multiple studies simultaneously?

Research Coordinators often juggle several studies at once, which can present challenges such as balancing competing deadlines, ensuring compliance with regulatory requirements, and managing communication among diverse stakeholders. Staying organized with detailed documentation and proactive scheduling is essential to prevent protocol deviations. Effective collaboration with principal investigators, sponsors, and clinical staff also helps to navigate unexpected changes and maintain study integrity.

What are Research Coordinators?

Research Coordinators are professionals responsible for managing and overseeing research projects, often in academic, medical, or clinical settings. They help design studies, ensure compliance with regulations, recruit and communicate with participants, and manage data collection and documentation. Research Coordinators play a crucial role in keeping projects organized, on schedule, and in accordance with ethical and institutional guidelines. They often serve as a bridge between principal investigators, participants, and regulatory bodies.

What is the difference between Research Coordinator vs Research Assistant?

AspectResearch CoordinatorResearch Assistant
Required CredentialsBachelor's degree often required; some roles prefer or require a master'sTypically an undergraduate student or recent graduate; some roles may require a bachelor's degree
Work EnvironmentLeads study activities, manages protocols, interacts with stakeholdersSupports data collection, literature review, and administrative tasks
Employer & Industry UsageUsed in clinical, academic, and industry research settingsCommonly found in academic labs and research projects

The Research Coordinator generally has more responsibilities, including managing study protocols and liaising with stakeholders, while the Research Assistant provides support with data collection and administrative tasks. Both roles are essential in research projects but differ in scope and level of responsibility.

More about Research Coordinator jobs
What are the most commonly searched types of Research jobs in Columbus, OH? The most popular types of Research jobs in Columbus, OH are:
What are popular job titles related to Research Coordinator jobs in Columbus, OH? For Research Coordinator jobs in Columbus, OH, the most frequently searched job titles are:
What job categories do people searching Research Coordinator jobs in Columbus, OH look for? The top searched job categories for Research Coordinator jobs in Columbus, OH are:
What cities near Columbus, OH are hiring for Research Coordinator jobs? Cities near Columbus, OH with the most Research Coordinator job openings:
Research Coordinator jobs near you
Clinical Research Coordinator

Clinical Research Coordinator

Centricity Research

Columbus, OH • On-site

$23.50 - $31.25/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 24 days ago

Job description

Join Us at Centricity Research!
Centricity Research is one of the largest clinical research networks in North America. We are a fully centralized Integrated Research Organization (IRO) specializing in conducting Phase I-IV clinical trials in over 35 therapeutic areas: inpatient and outpatient; pharmaceutical, biotechnology, and medical device trials.
About the role
We are seeking a Clinical Research Coordinator I (CRC I) to join our research team. In this role, you will support the successful execution of clinical studies by performing a mix of administrative and clinical responsibilities. You will work closely with Investigators and the broader research team to ensure study activities are organized, compliant, and aligned with protocol requirements. This is an excellent opportunity to build your skills in clinical research and contribute to meaningful studies that impact patient care.
What you'll do
Study Coordination & Participant Safety
  • Conduct study visits in accordance with protocol, GCP, SOPs, and regulatory requirements
  • Ensure participant safety and well-being, reporting and documenting adverse events per protocol and regulations
  • Perform clinical procedures such as vitals, ECGs, sample collection/processing, and investigational product handling

Recruitment, Screening & Enrollment
  • Support recruitment strategies to identify and enroll eligible participants
  • Conduct participant screening according to protocol inclusion/exclusion criteria
  • Guide participants through the informed consent process and ensure proper documentation
  • Schedule and coordinate study visits throughout the participant lifecycle

Study Execution & Data Integrity
  • Accurately complete study documentation, regulatory records, and periodic reports
  • Prepare for and support monitoring visits, audits, and inspections
  • Perform regular quality control (QC) checks on study data and source documents
  • Collaborate with investigators, management, and sponsors to ensure study compliance and accuracy
  • Contribute to site start-up activities, including feasibility questionnaires (FQs) and pre-study visits (PSVs)

Quality, Compliance & Site Support
  • Prepare for monitoring visits, audits, and maintain regulatory files
  • Perform regular quality control checks on source data and documents
  • Support lab supply inventory, equipment maintenance, and administrative needs
  • Assist with community engagement and outreach events as needed

You Might Be a Great Fit If You:
  • Have a bachelor's degree in a health, science, or research-related field (or equivalent combination of education and experience)
  • Have 2-4 years of experience in a healthcare setting and are comfortable with clinical tools like blood pressure monitors, ECG machines, and weight scales (nice to have, but not required)
  • Have phlebotomy experience - or are open to learning it where permitted by law (we'll provide the training).
  • Understand basic medical terminology, or are eager to learn it quickly
  • Are passionate about contributing to clinical trials that impact global health
  • Are organized, detail-oriented, and skilled at multitasking in a fast-paced environment
  • Are proactive, collaborative, and take ownership of your work
  • Value open communication and thrive in a team-driven environment

Why Centricity Research?
Our Mission
We connect people to scientific advancements through groundbreaking research within a deeply human experience.
Our Core Values
  • Quality: We aim for excellence and integrity in everything we do - because lives depend on it.
  • Care: We show up for each other, our customers, and our mission - always going the extra mile.
  • Be the Change You Seek: We're adaptable, forward-thinking, and constantly improving - for the betterment of all.
  • One Team: We collaborate, support one another, and succeed together.
  • Grow for Good: We grow with purpose - to expand access to research and improve global health.
  • Own It: We take initiative, deliver results, and follow through - with passion and accountability.

Benefits
  • Comprehensive health, dental, and vision insurance
  • Enhanced EAP - mental health support
  • Flexible PTO + paid holidays
  • Continuing education reimbursement
  • 401(k) / RRSP with company match and immediate vesting

Ready to Apply?
We'd love to hear from you - apply now!
We're an equal opportunity employer committed to building a diverse and inclusive workplace. We welcome applicants from all backgrounds and will provide accommodations during the hiring process upon request.

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