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Clinical Research Project Coordinator Jobs in Columbus, OH

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 ...

Actalent

Clinical Research Associate I

Westerville, OH

$25 - $27/hr

... clinical research of Gene Therapy products. This is a long-term career opportunity and we are ... coordination across internal teams and external partners. The position supports translational ...

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Clinical Research Project Coordinator information

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$21.7K

$61.2K

$89.8K

How much do clinical research project coordinator jobs pay per year?

As of May 28, 2026, the average yearly pay for clinical research project coordinator in Columbus, OH is $61,205.00, according to ZipRecruiter salary data. Most workers in this role earn between $50,700.00 and $68,600.00 per year, depending on experience, location, and employer.

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

To thrive as a Clinical Research Project Coordinator, you need a solid understanding of clinical research methodologies, project management, and regulatory compliance, typically supported by a bachelor’s degree in a health or science field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like CCRC or CCRP are commonly required. Exceptional organizational skills, attention to detail, and strong interpersonal communication help manage timelines, collaborate with stakeholders, and ensure protocol adherence. These competencies are crucial for maintaining study integrity, meeting regulatory standards, and ensuring successful project delivery in complex research environments.

What are some common challenges faced by Clinical Research Project Coordinators, and how can they be managed effectively?

Clinical Research Project Coordinators often encounter challenges such as balancing multiple studies simultaneously, ensuring regulatory compliance, and maintaining clear communication among diverse stakeholders. Effective time management, attention to detail, and the ability to adapt to changing protocols are essential in this role. Building strong relationships with research staff, principal investigators, and sponsors can help streamline processes and resolve issues quickly. Staying organized and proactively addressing potential obstacles can significantly contribute to the success of clinical research projects.

What does a Clinical Research Project Coordinator do?

A Clinical Research Project Coordinator manages and oversees the daily operations of clinical research studies. Their responsibilities include coordinating study activities, ensuring compliance with regulatory requirements, maintaining accurate documentation, scheduling participant visits, and communicating with research teams and sponsors. They play a crucial role in ensuring that research projects run smoothly, on time, and within budget while upholding ethical standards.

What is the difference between Clinical Research Project Coordinator vs Clinical Research Associate?

AspectClinical Research Project CoordinatorClinical Research Associate
CredentialsBachelor's degree in life sciences or related field; certifications like CCRP are a plusTypically requires similar degrees; certifications like CRA or CCRP are common
Work EnvironmentManages study logistics, coordinates with teams, and oversees daily activities at research sitesMonitors clinical trials, ensures compliance, and conducts site visits
Employer & Industry UsageUsed by hospitals, research institutions, and pharmaceutical companies for study coordinationPrimarily employed by CROs, pharmaceutical companies, and biotech firms for trial monitoring

While both roles support clinical research, the Clinical Research Project Coordinator focuses on managing study operations and logistics, whereas the Clinical Research Associate primarily monitors trial compliance and site performance. Both roles require similar educational backgrounds and certifications, but their daily responsibilities and work environments differ.

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

Research Regulatory Coordinator - RI Pulmonary Med

Nationwide Children's Hospital

Columbus, OH • On-site

$23.50 - $31.25/hr

Full-time

Posted 22 days ago

Nationwide Children's Hospital rating

7.1

Company rating: 7.1 out of 10

Based on 126 frontline employees who took The Breakroom Quiz

431st of 989 rated hospitals

Job description

Overview:
Job Description Summary:
Assists with the administrative components required to ensure compliance in the regulatory processes for a clinical research project.
Job Description:
Essential Functions:
  • Creates the initial study administrative binder required for the clinical research project. Maintains study binders, files documents timely, and reviews binders prior to monitor visits to ensure completeness.
  • Prepares, submits, and maintains IRB related documents.Ensures accuracy and congruency between IRB, regulatory documents, study documents and grants system.
  • Confirm all investigators, staff and departments to be used for the study. Collects CV's and licenses and confirms that IRB training requirements have been met. Maintains master file of current CV's and licenses.
  • Collects and stores regulatory documents required by the clinical research project in compliance with federal and local regulations and guidelines.
  • Keeps site documents up to date (IRB roster, lab certificates, etc.). Oversees document retrieval and archival process at study termination.
  • Works with marketing and research staff to ensure studies utilizing recruitment tactics are posted appropriately.

Education Requirement:
Associates degree or equivalent experience in medical/science field.
Licensure Requirement:
(not specified)
Certifications:
(not specified)
Skills:
Strong administrative skills and attention to detail.
Excellent computer skills.
Knowledge of medical terminology and diseases.
Ability to multi-task; customer focused personality with strong organizational and prioritization skills.
Working knowledge of IRB and regulatory processes and systems.
Current knowledge of Federal regulations (FDA, GCP, NIH, DHHS, ICH GCP), and study protocols.
Experience:
Six months research experience, preferred.
Physical Requirements:
OCCASIONALLY: Bend/twist, Driving motor vehicles (work required) *additional testing may be required, Reaching above shoulder, Squat/kneel
FREQUENTLY: Lifting / Carrying: 0-10 lbs, Lifting / Carrying: 11-20 lbs, Pushing / Pulling: 0-25 lbs, Pushing / Pulling: 26-40 lbs, Sitting, Standing, Walking
CONTINUOUSLY: Audible speech, Computer skills, Decision Making, Depth perception, Flexing/extending of neck, Hand use: grasping, gripping, turning, Hearing acuity, Interpreting Data, Peripheral vision, Problem solving, Repetitive hand/arm use, Seeing - Far/near
Additional Physical Requirements performed but not listed above:
(not specified)
"The above list of duties is intended to describe the general nature and level of work performed by individuals assigned to this classification. It is not to be construed as an exhaustive list of duties performed by the individuals so classified, nor is it intended to limit or modify the right of any supervisor to assign, direct, and control the work of employees under their supervision. EOE M/F/Disability/Vet"

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About Nationwide Children's Hospital

Sourced by ZipRecruiter

Nationwide Children's Hospital, established in 1894, is a leading pediatric healthcare system based in Columbus, Ohio, United States. They serve as a primary pediatric network, providing wellness, preventive, diagnostic, treatment, and rehabilitative care for infants, children, adolescents, and adults with congenital disease. Being the third-largest pediatric hospital in the nation, Nationwide Children's Hospital prides itself on its relentless commitment to children and their families, driven by their core values of respect, integrity, determination, empathy, and solidarity. The institution's comprehensive mission is to enhance the health of children by providing high-quality, family-centered care, conducting groundbreaking research, advocating for pediatric health, and training top healthcare professionals.

Industry

Hospitals

Company size

10,000+ Employees

Headquarters location

Columbus, OH, US

Year founded

1892

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