100 research coordinator jobs at 28 companies in Covington, KY
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Clinical Research Coordinator II
Cincinnati, Ohio, United States
OnsiteFull Time
2+ YOERequires a bachelor's degree and 2 years' life science experience, or equivalent education and experience, plus 1 year of clinical research coordinator experience, medical terminology, Microsoft Office, English, and leadership skills.
Microsoft Office, fax, copier, multi-line telephone, telephone, ECG
3w
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Clinical Research Coordinator II
Cincinnati, Ohio, United States
OnsiteFull Time
3+ YOE3+ years clinical research coordination experience, knowledge of GCP and FDA regulations, able to manage multiple trials, perform blood draws/ECGs/specimen processing, obtain informed consent, and maintain regulatory documentation.
1w
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Senior Clinical Research Coordinator
Dayton or Beavercreek
OnsiteFull Time
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
1mo
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Entry-Level Research Project Coordinator
Cincinnati, Ohio, United States
OnsiteFull Time
Bachelor's in life sciences, strong computer/organizational/time-management skills; research experience preferred; Medpace training provided.
3mo
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Clinical Research Project Coordinator - Oncology
Cincinnati, Ohio, United States
OnsiteFull Time
Bachelor's degree in life sciences required; strong computer, organizational, and time management skills; research experience preferred; office-based role with training provided.
1mo
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Clinical Research Coordinator III
Cincinnati, Ohio, United States
$57k-$62k/yr OnsiteFull Time
1+ YOEBachelor's in related field plus 1+ year related experience (or Master's); knowledge of regulatory compliance, data management, consent processes, and study conduct.
2w
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Clinical Research Coordinator
Kettering, Ohio, United States
OnsiteFull Time
Coordinate clinical trials from start-up to closeout, maintain regulatory compliance (GCP/IRB/FDA), manage regulatory documents, enroll participants, process specimens, and use EMR/EDC and Microsoft Office.
EMR, EDC, Vendor Portals, Microsoft Word, Microsoft Excel, Microsoft Outlook, OneDrive, Teams
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Senior Clinical Research Coordinator Full Time - 1st Shift
Dayton, Ohio, United States
OnsiteFull Time
3+ YOEBachelor’s degree in health sciences or related field; strong organization, EDC proficiency, independence, and compliance with clinical research regulations. Three-plus years of clinical research experience preferred.
Electronic Data Capture (EDC)
3mo
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Clinical Research Coordinator - Ophthalmology
Blue Ash, Ohio, United States
OnsiteFull Time
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
1mo
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Research & Visualization Coordinator
Cincinnati, Ohio, United States
OnsiteFull Time
1+ YOEBachelor's in design/visualization/communications, 1–3 years design-focused experience, proficiency with Adobe Illustrator, Adobe InDesign, data visualization platforms, Microsoft Excel and PowerPoint, strong written and visual communication skills.
Adobe Illustrator, Adobe InDesign, Microsoft Excel, Microsoft PowerPoint
1mo
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Research Assistant
Cincinnati, Ohio, United States
OnsiteFull Time
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
3mo
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Clinical Research Project Coordinator - Oncology
Cincinnati, Ohio, United States
OnsiteFull Time
0+ YOEBachelor’s in Life Sciences; strong computer, organizational, and time management skills; research experience preferred.
2d
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RN Research Nurse
Edgewood, Kentucky, United States
OnsiteFull Time
2+ YOEBachelor's degree in nursing, nursing license, and 2 years of nursing experience. Must coordinate clinical research, follow protocols and regulations, manage data, and prioritize multiple deadlines.
Standard Operating Procedures (SOPs), Institutional Review Board (IRB), HIPAA, Office for Human Research Protections (OHRP), US Food and Drug Administration (FDA), Good Clinical Practices, Good Laboratory Practices
1mo
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Clinical Research Assistant
Cincinnati, Ohio, United States
OnsiteFull Time
Perform vitals, ECGs, specimen processing, complete source documentation and case report forms, assist coordinators with subject visits, comply with GCP. High school diploma or equivalent; 1 year clinical experience preferred but newly certified applicants accepted.
2w
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Clinical Research Professional, Department of Neurology & Rehabilitation Medicine, MS
Cincinnati, Ohio, United States
$64k/yr OnsiteFull Time
1+ YOEBachelor's in a related field (or 5 years' relevant experience), 1 year related experience, ability to screen patients, maintain regulatory/IRB documentation, coordinate clinical research, and perform clinical procedures.
SuccessFactors
3mo
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PERMIT COORDINATOR
Erlanger, Kentucky, United States
OnsiteFull Time
Coordinate permit processes, manage schedules, maintain spreadsheets, research permit requirements; strong communication; in-office in Erlanger, KY.
Microsoft Office, Excel, Word, Databases
2w
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Institutional Review Board Coordinator
Cincinnati, Ohio, United States
OnsiteFull Time
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
1mo
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Project Coordinator
Dayton, Ohio, United States
OnsiteFull Time
1+ YOEBachelor's in STEM with 1-2 years scientific/analytical/research experience, proficiency with Microsoft Office, strong communication, autonomous work ability, and logistics/equipment familiarity.
Microsoft Excel, Outlook, PowerPoint, Word, Access
1mo
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Project Coordinator
Dayton, Ohio, United States
OnsiteFull Time
1+ YOEBachelor's in STEM,1+ years experience in scientific/analytical/research settings,proficiency with Microsoft Office,strong written/verbal communication,ability to manage projects,experience with protocol/document compliance and logistics.
Microsoft Excel, Microsoft Outlook, Microsoft PowerPoint, Microsoft Word, Microsoft Access, Scientific and Technical Information (STINFO)
4w
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Project Coordinator
Dayton, Ohio, United States
OnsiteFull Time
1+ YOEBachelor's in STEM and 1-2 years research or scientific experience; proficiency with Microsoft Office; strong communication, organization, and project management skills; U.S. citizenship and ability to pass Tier 1 background check.
Microsoft Excel, Microsoft Outlook, Microsoft PowerPoint, Microsoft Word, Microsoft Access
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