18 clinical research coordinator entry level jobs at 4 companies in Springfield, OH
1mo
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Clinical Research Coordinator
Columbus, Ohio, United States
OnsiteFull Time
Bachelor's degree required. Coordinates clinical research studies under investigator supervision, applying GCP guidelines and federal regulations while managing participants, data, documentation, reporting, and compliance.
Good Clinical Practice (GCP)
2mo
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Clinical Research Coordinator
Columbus, Ohio, United States
OnsiteFull Time
Bachelor's degree required. Coordinate clinical research studies under PI supervision, recruit and consent participants, collect and record study data per GCP and regulations, assist with monitoring and audit preparedness.
6d
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Senior Clinical Research Coordinator
Columbus, Ohio, United States
OnsiteFull Time
2+ YOEBachelor's degree, 2 years of direct human subjects and clinical research experience, strong communication and computer skills, and knowledge of EMR and Microsoft systems. Clinical research certification preferred.
EMR, Microsoft
1w
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Clinical Research Coordinator- Neurology
Kenny Rd or Dublin or New Albany or Powell or Upper Arlington or Columbus
OnsiteFull Time
1+ YOEBachelor's in a relevant field or equivalent, 1+ year clinical research experience, clinical research certification preferred, background check required, patient-facing onsite role, Microsoft Office experience desired.
Microsoft Software applications
1mo
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Clinical Research Coordinator Float-Clinical Trials Management Office
Columbus or Columbus or New Albany or Dublin or Columbus or Upper Arlington
OnsiteFull Time
1+ YOEBachelor's in a related field or equivalent, 1 year clinical research experience, computer proficiency; experience coordinating clinical trials and clinical research certification preferred.
Microsoft applications, RedCap, Medidata, Rave, Workday
2mo
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Clinical Research Coordinator - Oncology
Columbus, Ohio, United States
OnsiteFull Time
1+ YOEBachelor's in biological/health/social sciences or equivalent; 1 year clinical research experience required; clinical research certification desired; knowledge of medical terminology and Microsoft Office; strong verbal and written communication skills.
Workday, Microsoft Office
1mo
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Clinical Research Coordinator-Clinical Trials Management Office
Hilliard or Dublin or Powell or New Albany or Columbus
OnsiteFull Time
1+ YOEBachelor's in a related field (or equivalent), 1+ year clinical research experience, patient-facing coordination, informed consent, data collection, and familiarity with regulatory compliance.
Microsoft Software applications
6d
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Clinical Research Coordinator-Hematology
Columbus, Ohio, United States
OnsiteFull Time
1+ YOEBachelor's degree in biological, health, social, or medical sciences, or equivalent education and experience, plus 1 year of relevant clinical research experience; 2–4 years preferred.
1w
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Clinical Research Coordinator (HS)- Neurology
Columbus, Ohio, United States
OnsiteFull Time
1+ YOECoordinate and perform daily clinical research activities, recruit and consent patients, schedule procedures, collect/process samples, ensure IRB/FDA compliance; bachelor’s in biological/health/social sciences or equivalent and 1 year relevant experience required.
3w
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Clinical Research Coordinator II - RI Rheumatology
Columbus, Ohio, United States
OnsiteFull Time
1.5+ YOEAssociate's degree or equivalent, 18 months clinical research or healthcare experience, CRA/CRC preferred, knowledge of medical terminology, strong communication, analytical and organizational skills.
1w
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Senior Clinical Research Coordinator
Columbus, Ohio, United States
OnsiteFull Time
2+ YOEBachelor's degree, two years of direct human subjects and clinical research experience, strong communication and computer skills, and the ability to manage multiple projects; certification is preferred.
Good Clinical Practice (GCP), Electronic Medical Records (EMR), Microsoft
3w
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Clinical Research Coordinator I
Columbus, Ohio, United States
OnsiteFull Time
Manages clinical study activities per ICH/GCP; recruits, consents, enrolls subjects; collects and manages research data; processes human specimens; performs CLIA-waived assessments.
5d
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Clinical Research Coordinator Social & Behavioral Sciences I
Columbus, Ohio, United States
OnsiteFull Time
Associate's degree or equivalent certification/experience required; bachelor's preferred. Requires CNA, PCA, LPN, MA, or equivalent, with clinical research or healthcare experience preferred.
PCs, word processing, data management software
4d
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Clinical Research Coordinator I (CRC I)
Columbus, Ohio, United States
$50k-$52k/yr OnsiteFull Time
1+ YOERequires 1+ year direct clinical research coordination experience, hands-on phlebotomy, clinical trial protocol knowledge, participant recruitment and documentation skills, GCP/SOP knowledge, and a relevant bachelor's degree or equivalent experience.
ECG, Electronic Data Capture (EDC)
1mo
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Clinical Research Coordinator I - Emergency Medicine
Columbus, Ohio, United States
OnsiteFull Time
Manage clinical study activities per ICH/GCP, recruit/consent subjects, collect/process specimens, maintain regulatory documentation. Requires associate degree or equivalent, CNA/PCA/LPN/MA or equivalent, CRC/CRA certification after hire.
2w
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Clinical Research Coordinator I - RI Pulmonary Med
Columbus, Ohio, United States
OnsiteFull Time
Manages clinical study activities per ICH/GCP, recruits/consents subjects, collects and manages study data and specimens, completes CRFs and regulatory documentation. Associate degree or equivalent required; CRA/CRC certification after hire; CNA/PCA/LPN/MA required.
1mo
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Clinical Research Coordinator I - RI Behav Trials Off
Columbus, Ohio, United States
OnsiteFull Time
Manages clinical study activities per ICH/GCP and SOPs; recruits/consents subjects, collects and manages data and specimens, performs CLIA-waived testing; associate degree or equivalent and CNA/PCA/LPN/MA required; CRC/CRA certification after hire required.
1w
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Senior Research Regulatory Coordinator - RI Gene Ther
Columbus, Ohio, United States
OnsiteFull Time
2+ YOEBachelor's degree or equivalent medical/science experience and two years of clinical research experience required. Requires regulatory knowledge, computer skills, organization, prioritization, and attention to detail; CCRP preferred.
Institutional Review Board (IRB), Investigational New Drug (IND), U.S. Food and Drug Administration (FDA), NIH, DHHS, ICH GCP
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