13 study coordinator jobs at 6 companies in Newark, OH
1mo
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Clinical Research Coordinator
Columbus, Ohio, United States
OnsiteFull Time
1+ YOEBachelor's degree required. Coordinates clinical research per GCP, recruits and consents participants, maintains study records, assists with reporting and audit preparedness. Strong communication and computer (EMR, Microsoft) skills.
Electronic Medical Records (EMR), Microsoft
1mo
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SIOPurchasing Coordinator-SW
Delaware, Ohio, United States
OnsitePart Time
Customer-service oriented, strong communication, attention to detail, professionalism, willing to learn; preference for juniors/seniors, business/accounting majors, and federal work-study; must be authorized to work in the US.
1mo
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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.
4w
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Video Coordinator/Content Creator
Columbus, Ohio, United States
$11/hr OnsitePart Time
Federal Work-Study eligibility, ability to record and edit video and design graphics, availability to work 12-16 hours/week with weekend and travel availability.
4w
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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.
2mo
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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.
3w
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EEG Technologist II - Neuro Special Studies Coordinator
Columbus, Ohio, United States
OnsiteFull Time
3+ YOEAssociate degree or equivalent, ABRET registration (R EEG T), BLS, 3 years EEG experience, ability to prepare reports, troubleshoot artifacts, monitor patients, and perform investigational procedures.
2w
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Research Associate- Pulmonary Critical Care and Sleep
Columbus, Ohio, United States
OnsiteFull Time
Experience with cell culture, immunoblotting, DNA/RNA preparation, immunocytochemistry, mouse studies, and independent molecular and biochemical experiments; requires data analysis and laboratory coordination.
2w
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Virtual Obs RN - Hybrid, Full Time, Nights - Pickerington
Pickerington, Ohio, United States
HybridFull Time
0+ YOERequires an Ohio RN license and American Heart Association BLS. Nursing field of study; no prior experience required. Provides virtual care coordination, assessment, teaching, coaching, and documentation.
2w
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Virtual Obs RN - Hybrid, Pickerington
Columbus or Pickerington
HybridFull Time
0+ YOEOhio RN license and American Heart Association BLS required. Nursing field of study accepted; no prior experience required. Strong assessment, care planning, coordination, teaching, coaching, and quality improvement skills needed.
2w
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Virtual Obs RN - Hybrid, Pickerington
Pickerington, Ohio, United States
OnsiteFull Time
0+ YOEOhio RN license and American Heart Association BLS required. Nursing field of study. No prior experience required; role involves virtual care coordination, assessment, patient education, team coaching, and care planning.
2w
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Virtual Obs RN - Onsite, Part time, nights - Pickerington
Pickerington or United States
OnsitePart Time
Ohio RN license and American Heart Association BLS required. Nursing field of study; no prior experience required. Must coordinate care, assess patients, document interventions, educate patients, and coach care teams.
HRO
2mo
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Clinical Research & IRB Specialist
Zanesville, Ohio, United States
OnsitePart Time
Associate degree or paralegal/legal studies program completion, progressive experience in legal/compliance/contracts/regulatory support, contract review and coordination experience, training/oversight ability, knowledge of regulatory concepts, strong organization and communication, proficiency with office software and document management systems.
ClinicalTrials.gov, Trial Master File (TMF)