50 clinical research coordinator entry level jobs at 7 companies in Covington, KY

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Clinical Research Coordinator II
Cincinnati, Ohio, United States
OnsiteFull Time
Velocity Clinical Research
Velocity Clinical Research: Integrated clinical research site organization conducting medical trials.
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
1mo
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Clinical Research Project Coordinator - Ophthalmology
Cincinnati, Ohio, United States
OnsiteFull Time
Medpace
MedpaceNasdaq: MEDP: Full-service clinical contract research organization for medical development.
Bachelor's in life sciences required, strong computer/organizational skills, research experience preferred; training provided for candidates without clinical research experience.
3mo
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Clinical Research Project Coordinator - Oncology
Cincinnati, Ohio, United States
OnsiteFull Time
Medpace
MedpaceNASDAQ: MEDP: Conducts clinical trials for biotechnology and pharmaceutical companies.
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 III, Various Departments
Cincinnati, Ohio, United States
$57k-$62k/yr OnsiteFull Time
Cincinnati Children's
Cincinnati Children's: Provides specialized pediatric healthcare and conducts clinical research.
1+ YOEBachelor's degree in a related field plus 1 year of related experience, or a master's degree. Requires organization, communication, problem-solving, multitasking, attention to detail, and Microsoft Office proficiency.
Microsoft Office, REDCap, Medidata, OnCore
3mo
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Clinical Research Project Coordinator - Oncology
Cincinnati, Ohio, United States
OnsiteFull Time
Medpace
MedpaceNASDAQ: MEDP: Full-service clinical research organization for pharmaceutical and biotechnology industries.
0+ YOEBachelor’s in Life Sciences; strong computer, organizational, and time management skills; research experience preferred.
2mo
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Clinical Research Assistant
Cincinnati, Ohio, United States
OnsiteFull Time
CTI Clinical Trial and Consulting Services
CTI Clinical Trial and Consulting Services: Clinical trial management and consulting for life sciences companies.
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.
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Clinical Research Professional, Department of Neurology & Rehabilitation Medicine, MS
Cincinnati, Ohio, United States
$64k/yr OnsiteFull Time
University of Cincinnati
University of Cincinnati: Public research university providing academic degrees and healthcare services.
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
2mo
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Research Assistant
Cincinnati, Ohio, United States
OnsiteFull Time
Gastro Health
Gastro Health: Provides specialized gastroenterology and digestive healthcare 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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RN Research Nurse
Edgewood, Kentucky, United States
OnsiteFull Time
St. Elizabeth Healthcare
St. Elizabeth Healthcare: Providing comprehensive medical care and hospital services.
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