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71 clinical research coordinator jobs at 11 companies in Kettering, OH

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Clinical Research Coordinator
New Carlisle, Ohio, United States
OnsiteFull Time
Tekton Research
Tekton Research: Physician-led U.S. clinical research site network running Phase 1–4 trials for sponsors, CROs, and biotech companies.
0.5+ YOEHigh school diploma/GED required; 6–12 months clinical research experience, GCP and regulatory knowledge, phlebotomy and specimen processing experience, EDC and Microsoft Office proficiency.
Electronic Data Capture (EDC), Clinical Trial Management Systems (CTMS), Microsoft Office
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3w
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Clinical Research Coordinator II
Cincinnati, Ohio, United States
OnsiteFull Time
Velocity Clinical Research
Velocity Clinical Research: Clinical research site organization conducting Phase I–IV trials for pharma and biotech companies across U.S. and Europe.
2+ YOERequires a bachelor's degree and 2 years' relevant life science experience, or equivalent combinations, plus 1 year of Clinical Research Coordinator experience, medical terminology, Microsoft Office, English, and leadership skills.
Microsoft Office, fax, copier, multi-line telephone
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3w
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Senior Clinical Research Coordinator
Dayton or Beavercreek
OnsiteFull Time
One GI
One GI: Physician-led gastroenterology management services organization supporting independent GI practices and their patients.
5+ YOEAssociate's or Bachelor's in scientific/healthcare field, 5+ years clinical research or healthcare experience, ability to perform blood draws/EKGs, strong GCP/FDA knowledge, CTMS/EDC proficiency, mentoring experience.
CTMS, EDC
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Clinical Research Coordinator IV - Allergy Department
Cincinnati, Ohio, United States
$61k-$78k/yr OnsiteFull Time
Cincinnati Children's Hospital Medical Center
Cincinnati Children's Hospital Medical Center: Pediatric academic medical center and research institution.
3+ YOEBachelor's degree in a related field and 3+ years of related experience, or a master's degree and 2 years of experience. Clinical Research Coordinator certification required within 18 months of external hire.
Case Report Forms (CRFs), Data Dictionary, Electronic Medical Records (EMR)
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Clinical Research Coordinator
Kettering, Ohio, United States
OnsiteFull Time
Dayton Physicians Network
Dayton Physicians Network: Independent physician-owned Ohio medical network providing cancer, urology, imaging, and clinical research services.
Bachelor's degree in nursing or a health-related field preferred; clinical research experience preferred. Familiarity with GCP and IRB requirements, EMRs, EDCs, vendor portals, and Microsoft Office required.
EMR, EDC, Vendor Portals, Microsoft Word, Microsoft Excel, Microsoft Outlook, Microsoft OneDrive, Microsoft Teams
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Clinical Research Project Coordinator - Ophthalmology
Cincinnati, Ohio, United States
OnsiteFull Time
Medpace
MedpaceNASDAQ: MEDP: Global full-service clinical contract research organization.
Bachelor's in life sciences required, strong computer/organizational skills, research experience preferred; training provided for candidates without clinical research experience.
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Clinical Research Coordinator (level dependent on experience)
Cincinnati, Ohio, United States
HybridFull Time
CTI Clinical Research Center
CTI Clinical Research Center: Privately held global contract research organization serving pharmaceutical, biotechnology, and medical-device companies with clinical trials and consulting.
1+ YOERequires 1+ year clinical research or related medical/mental health experience and a bachelor's degree in life sciences or equivalent education and experience. CCRC, nursing degree, and ACLS preferred.
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Clinical Research Coordinator I
Cincinnati, Ohio, United States
OnsiteTemporary
Velocity Clinical Research
Velocity Clinical Research: Clinical research site organization conducting Phase I–IV trials for pharma and biotech companies across U.S. and Europe.
1+ YOERequires a bachelor's degree plus 1 year, associate's degree plus 2 years, or high school/technical education plus 3 years of life science experience; English, medical terminology, Microsoft Office, communication, and organizational skills required.
Microsoft Office, fax, copier, multi-line telephone
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Clinical Research Project Coordinator - Oncology
Cincinnati, Ohio, United States
OnsiteFull Time
Medpace
MedpaceNASDAQ: MEDP: Global full-service clinical contract research organization.
Bachelor's degree in life sciences required; strong computer, organizational, and time management skills; research experience preferred; office-based role with training provided.
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Clinical Research Coordinator - Ophthalmology
Blue Ash, Ohio, United States
OnsiteFull Time
Cincinnati Eye Institute
Cincinnati Eye Institute: Private ophthalmology practice serving Greater Cincinnati patients with medical, surgical, and comprehensive eye care.
1+ YOEHigh school graduate; CCRC or higher; 1+ year ophthalmic/optometric experience; knowledge of GCP/CITI; strong Excel/Word; willing to travel; team oriented.
GCP, CITI certification, IRB, electronic data capture, case report forms, Microsoft Word, Microsoft Excel, Microsoft Access
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Clinical Research Project Coordinator - Oncology
Cincinnati, Ohio, United States
OnsiteFull Time
Medpace
MedpaceNASDAQ: MEDP: Global full-service clinical contract research organization.
0+ YOEBachelor’s in Life Sciences; strong computer, organizational, and time management skills; research experience preferred.
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Clinical Research Project Manager, COM CCTST
Cincinnati, Ohio, United States
$101k/yr HybridFull Time
University of Cincinnati College of Medicine
University of Cincinnati College of Medicine: Public medical school training physicians and scientists while advancing biomedical research and patient care.
5+ YOEBachelor's degree and five years of related experience required, with academic or clinical research experience preferred. Requires data management, analytics, workflow, and research program coordination skills.
R, Python, SQL, REDCap, Tableau, Power BI, SuccessFactors
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2mo
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Research Assistant
Cincinnati, Ohio, United States
OnsiteFull Time
Gastro Health
Gastro Health: Private U.S. gastroenterology medical group treating patients with digestive and liver disorders through physicians, procedures, and ancillary services.
High school diploma required; assists clinical research coordinators, screens and registers participants, maintains lab inventory, processes and ships labs, completes EDC, and supports study documentation and closeout.
EDC, Real Time
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4w
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Institutional Review Board Coordinator
Cincinnati, Ohio, United States
OnsiteFull Time
Good Samaritan Hospital
Good Samaritan Hospital: Catholic nonprofit teaching and tertiary hospital serving patients in Greater Cincinnati and the Ohio-Indiana-Kentucky Tri-State region.
3+ YOEBachelor's degree,3+ years clinical research/IRB/healthcare administration experience,medical terminology knowledge,Microsoft Office (Word,Excel) proficiency,typing 55-60 WPM preferred,strong organization and communication.
Microsoft Office Suite, Microsoft Word, Microsoft Excel
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