Inside Higher Ed · 3 weeks ago
Clinical Research Coordinator - CCC | Clinical Trials Office
The Ohio State University is a prominent academic institution, and they are seeking a Clinical Research Coordinator to perform daily clinical research activities in accordance with approved protocols. The role involves patient assessment, enrollment, education, compliance monitoring, and data collection within the Clinical Trials Office.
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Responsibilities
Assist with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols
Identify, pre-screen and enroll patients
Obtain informed consent and ensure consent process is administered in compliance with regulatory and sponsor requirements
Educate patients and families of purpose, goals, and processes of clinical study
Coordinate scheduling and follow-through of patient care appointments, procedures, & other diagnostic testing in accordance with the study protocol
Assist with monitoring patients for adverse reactions to study treatment, procedure, or medication and notifies appropriate clinical professionals to evaluate patient response, identify the status of complications, & provide the appropriate level of care
Document unfavorable responses and notify research sponsors & applicable regulatory agencies
Assist with collecting, extracting, and entering clinical research data
Support activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state, and industry sponsor regulations
Assist with coordinating and preparing for internal and external audits and quality assurance reviews by IRB, federal or industry sponsors
Participate in activities to develop new case report forms for Investigator Initiated Trials (IITs) and contribute to the establishment of study goals to meet protocol requirements
Qualification
Required
Bachelor's Degree in biological sciences, health sciences, social sciences, or other related field, or an equivalent combination of education and experience required
One year of experience in a clinical research capacity (human subjects) is required
Computer skills required
Must be able to effectively communicate, both face-to-face and in writing, with clinical staff, research participants, and outside collaborators
Preferred
Knowledge of medical terminology desired
Clinical research certification from an accredited certifying agency desired
Experience using Microsoft Office Software applications desired
Benefits
Generous, fully paid tuition assistance program
Opportunity to apply and participate in the OSUCCC Professional Clinical Research Training Academy
Company
Inside Higher Ed
Inside Higher Ed is the online source for news, opinion, and jobs related to higher education.
Funding
Current Stage
Growth StageTotal Funding
unknown2022-01-10Acquired
2006-08-31Series Unknown
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